Items Standard Result Appearance Colorless,transparent liquid Complies Content% ≥99.90
Cas:100-51-6
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inquiryOur advantage: 1. 24hours to reply your E-mail; 2. Customized pakage; 3. Adequate stocks; 4. The competitive price owing to low labor cost and low material cost; 5.Market information trend share with customers; 6. Suggestion for purchase decisi
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inquiryProduct Information Chemical Name Benzyl alcohol CAS # 100-51-6 Formula C7H8O Molecular Weight 202-859-9 Items Specification
Cas:100-51-6
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inquiryZorui combines R&D, production and sales into its operations, While continuously providing high-quality raw materials, we also provide and optimize technical solutions for customers to achieve mutual benefit. We adhere to the "quality, integ
Cas:100-51-6
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inquiryHighly quality and large production Factory Chemwill Asia co.,Ltd is one of the leading manufacturer in CHINA. Our main production base is located in Xuzhou industry park. We produce a wide range of organics includin
Lonwin Industry group limited as a professional manufactor & exporter of chemical materials ,we totally haver more than 270 stuffs, we have been on this line for more than 9 years. Our chemical materials are exported to lot of countries and reg
Benzyl Alcohol (Chlorine-free/non-chlorine) Technology level Toluene oxidation production process, using toluene and air as raw materials, producing benzyl alcohol, with higher quality, more stable quality, technology level leading in domes
Cas:100-51-6
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inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
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inquiryhigh purity lowest price ANALYSIS SPECIFICATION RESULTS Assay HPLC 96.5%-101.5% 99.4% Identification
Product description: Product name Benzyl alcohol CAS number 100-51-6 Assay ≥99.9% Appearance Colorless transparent liquid Capacity 2000mt/year Application Essence, coating so
Cas:100-51-6
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inquiryUnique advantages for Benzyl alcohol Cas 100-51-6 Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Colorless liquid Storage:Store in 2-8℃ Package:25kg/drum,210kg/drum A
Cas:100-51-6
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inquiryhe company has advanced technology, as well as a large number of excellent R & D team, to provide customers from the grams to one hundred kilograms and tons of high-quality products, competitive prices and quality se T rvice Appearance:Whit
Benzyl alcohol Appearance & properties: colorless liquid, aromatic smell. Melting point (℃): -15.3 Relative Density (Water = 1): 1.04 (25 ℃) Boiling point (℃): 205.7 Vapor Density (Air = 1): 3.72 Relative Density (Water = 1): 1.0419
17-year experience in Phytochemicals Each product has passed very strict tests (NMR\MS\HPLC) Agents in 13 countries Certified by ISO 9001:2008 quality management system Leader Supplier of Botanical Reference Materials in China
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Cas:100-51-6
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inquiryCangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new api, intermedi
We would like to take this opportunity to give you a brief introduction of our company. We are one of the leading factories specialized in producing the following products: 1. Solid Epoxy Resin for Powder Coating such as E12, E14, E10 and the high q
Puritty: 99% Excellent quality with competitive price Fast delivery Appearance:colorless liquid Storage:stores in a well-ventilated, cool, dry area, out of direct sunlight. Package:200 kg/drum Application:antimicrobial, antipruritic Port:Shang
Cas:100-51-6
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Hebei yanxi chemical co. LTD. has expanded a compositive entity from initially only as a small manufacturer. The company dedicated to the development, production and marketing of chemicals. Main products are Titanium dioxide(CAS13463-67-7). Lead a
Cas:100-51-6
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inquiryName:Benzyl alcohol Name:Benzyl alcohol CAS no:100-51-6 Grade:Coating solvent Molecular formula: C7H8O Molecular weight: 108.1378 Product Quality 12 years of chemical raw materials Mature operation of the industry System stability
Cas:100-51-6
Min.Order:25 Kilogram
FOB Price: $1.0 / 2.0
Type:Other
inquiryChemical Name Benzyl alcohol CAS # 100-51-6 Formula C7H8O Molecular Weight 202-859-9 Items Specification Results Appearance Colorless transparent liquid Confirms Pu
Benzyl alcohol Melting point -15 °C Boiling point 205 °C Density 1.045 g/mL at 25 °C (lit.) Vapor density 3.7 (vs air) Vapor pressure 13.3 mm Hg (100 °C) Refractive index n20/D 1.539(lit.) FEMA 2137 | BENZYL ALCOHO
Cas:100-51-6
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturing
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Cas:100-51-6
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Type:Trading Company
inquiryMolecular formula: C7H8O Molecular weight: 108.14 Structural formula: CAS No.: 100-51-6 EC No.: 202-859-9 Properties Appearance & Characters: Benzyl alcohol is a kind of colorless transparent liquid; sending out slight fra
Appearance:Colourless liquid Storage:R.T Package:25kg/Barrel Application:Preparation of floral oils Transportation:Express/Sea/Air Port:Any port in China
Cas:100-51-6
Min.Order:100 Kilogram
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Type:Lab/Research institutions
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Cas:100-51-6
Min.Order:10 Gram
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Type:Trading Company
inquiryConditions | Yield |
---|---|
With sodium aluminum tetrahydride In tetrahydrofuran at 0℃; for 0.5h; | 100% |
With RuCl2(2-(diphenylphosphino)-N-(thiophen-2-ylmethyl)ethanamine)PPh3; hydrogen; sodium methylate In toluene at 100℃; under 37503.8 Torr; for 16h; Autoclave; | 100% |
With dichloro(benzene)ruthenium(II) dimer; 2-((di-p-tolylphosphino)methyl)-1-methyl-1H-imidazole; potassium tert-butylate; hydrogen In tetrahydrofuran at 100℃; under 37503.8 Torr; for 4.5h; | 99% |
Conditions | Yield |
---|---|
With Triethoxysilane; potassium fluoride for 36h; Product distribution; | 100% |
With n-butyllithium; 1-methoxycyclohexa-1,4-diene In tetrahydrofuran; Petroleum ether for 5h; Product distribution; Ambient temperature; | 100% |
With sodium tetrahydroborate In methanol; dichloromethane at 22℃; for 0.00166667h; also in other alcohols, also at other temperatures, also the reduction time required for 50percent reduction; | 100% |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; silica gel In hexane at 25℃; for 3h; | 100% |
With diisopropoxytitanium(III) tetrahydroborate In dichloromethane at -20℃; for 0.133333h; | 100% |
With trihexyl(tetradecyl)phosphonium decanoate*BH3 at 20℃; Product distribution / selectivity; | 99% |
Conditions | Yield |
---|---|
With C32H34BrN5ORu; potassium tert-butylate; hydrogen In tetrahydrofuran at 70℃; under 37503.8 Torr; for 4h; Reagent/catalyst; | 100% |
With C56H70Cl3N10Ru2(1+)*F6P(1-); potassium tert-butylate; hydrogen In tetrahydrofuran; dodecane at 70℃; under 37503.8 Torr; for 16h; Inert atmosphere; Glovebox; Autoclave; | 100% |
With C32H32Cl2N2P2Ru; hydrogen; sodium methylate In para-xylene; toluene at 5 - 100℃; under 37503.8 Torr; for 4h; Reagent/catalyst; Glovebox; | 100% |
Conditions | Yield |
---|---|
With dinitrogen tetraoxide In dichloromethane at -10℃; deprotection; | 100% |
poly(4-vinylpyridinium) p-toluenesulfonate In tetrahydrofuran; ethanol at 75℃; for 30h; Hydrolysis; | 99% |
With C24H20O3; toluene-4-sulfonic acid In tetrahydrofuran; methanol at 20℃; for 1h; | 99% |
benzyloxy-trimethylsilane
benzyl alcohol
Conditions | Yield |
---|---|
With dinitrogen tetraoxide In dichloromethane at -10℃; deprotection; | 100% |
With water; 1,1,1,3,3,3-hexamethyl-disilazane In dichloromethane at 20℃; for 0.25h; | 100% |
montmorillonite K-10 for 0.0166667h; Solid phase reaction; desilylation; microwave irradiation; | 99% |
Conditions | Yield |
---|---|
With tri-n-butyl-tin hydride; tetrakis(triphenylphosphine) palladium(0) In benzene at 5℃; | A n/a B 100% |
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In o-xylene at 80℃; for 24h; Inert atmosphere; | 100% |
Stage #1: benzyl formate With phenylsilane; C74H74Mn2N6P4 at 25℃; for 0.5h; Glovebox; Inert atmosphere; Stage #2: With sodium hydroxide In water at 25℃; for 2h; Glovebox; Inert atmosphere; | 99% |
Stage #1: benzyl formate With phenylsilane; (Ph2PPrPDI)Mn at 25℃; for 0.25h; Glovebox; Inert atmosphere; Stage #2: With sodium hydroxide In water at 25℃; for 2h; Catalytic behavior; Reagent/catalyst; Glovebox; | 88% |
Conditions | Yield |
---|---|
With C56H70Cl3N10Ru2(1+)*F6P(1-); potassium tert-butylate; hydrogen In tetrahydrofuran; dodecane at 70℃; under 37503.8 Torr; for 16h; Inert atmosphere; Glovebox; Autoclave; | 100% |
With dichloro(benzene)ruthenium(II) dimer; 2-((di-p-tolylphosphino)methyl)-1-methyl-1H-imidazole; potassium tert-butylate; hydrogen In tetrahydrofuran at 100℃; under 37503.8 Torr; for 2h; | 99% |
With C66H102N4OP2Ru; hydrogen In toluene at 105℃; under 22502.3 Torr; for 20h; Inert atmosphere; Glovebox; | 99% |
benzyl (1-chloroethyl) carbonate
A
benzyl 1-thiocyanoethylcarbonate
B
benzyl alcohol
Conditions | Yield |
---|---|
With tetrabutyl phosphonium bromide In acetone for 18.5h; Heating; | A 100% B 18% |
benzyl bromide
2-(trimethylsilyl)ethyl benzeneselenenate
benzyl alcohol
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran for 7h; Ambient temperature; | 100% |
With tetrabutyl ammonium fluoride In tetrahydrofuran for 7h; Product distribution; Ambient temperature; other alkyl halides, different reation times; | 100% |
benzyl 2-(2-hydroxypropyl)phenyl sulfone
A
3-methyl-1-oxobenzo-2,1-oxathiane
B
benzyl alcohol
Conditions | Yield |
---|---|
With sulfuric acid at 20℃; for 1h; | A 100% B 100% |
benzenesulphonylacetic acid benzyl ester
benzyl alcohol
Conditions | Yield |
---|---|
With ethanol; magnesium; mercury dichloride In tetrahydrofuran for 2h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); hypophosphorous acid; sodium hydrogencarbonate In ethanol for 5h; Heating; | 100% |
With tri(2-furyl)germane; triethyl borane In tetrahydrofuran at 20℃; for 1.5h; Reduction; | 93% |
With tri(2-furyl)germane; triethyl borane In tetrahydrofuran; hexane at 20℃; for 1.5h; | 93% |
With isopropyl alcohol at 20℃; for 12h; UV-irradiation; chemoselective reaction; | 86% |
With potassium phosphate; palladium diacetate; hydrazine hydrate In dimethyl sulfoxide; N,N-dimethyl-formamide at 20℃; for 8h; Green chemistry; | 78% |
Conditions | Yield |
---|---|
With silica gel; triethylamine In diethyl ether; Petroleum ether Substitution; Detrifluoroacetylation; | 100% |
methanol
Benzyl 3-phenylpropionate
A
3-phenylpropanoic acid methyl ester
B
benzyl alcohol
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A 100% B n/a |
ethanol
Benzyl 3-phenylpropionate
A
ethyl dihydrocinnamate
B
benzyl alcohol
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A 100% B n/a |
Benzyl 3-phenylpropionate
allyl alcohol
A
allyl 3-phenylpropionate
B
benzyl alcohol
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A 100% B n/a |
(2R,3S)-1-chloro-3-dibenzylamino-4-phenyl-2-butanol sulfuric acid salt
A
(2R,3S)-1-chloro-3-amino-4-phenyl-2-butanol sulfuric acid salt
B
benzyl alcohol
Conditions | Yield |
---|---|
With hydrogen; palladium hydroxide/carbon In methanol at 40℃; for 3h; | A 100% B n/a |
Li(1+)*ReMn(CO)9(CHO)(1-)=Li(ReMn(CO)9(CHO))
benzaldehyde
A
decacarbonylmanganeserhenium
B
benzyl alcohol
Conditions | Yield |
---|---|
In tetrahydrofuran under N2, benzaldehyde was added to soln. of Re-Mn-complex in THF at -78°C, warmed to -30°C, 5 min, quenched with aq. THF; | A 58% B 100% |
Conditions | Yield |
---|---|
With tetradecane In tetrahydrofuran under N2, 1.13 equiv of benzaldehyde in THF was added to soln. of Re-complex in THF, stirred for 1 h, water was added , extd. with ether, driedover Na2SO4, 1 equiv of tetradecane standard was added; solvent removed, dissolved in min. ether, hexane added, placed in freezer overnight, crystd., filtered, vac. dried; | A 100% B 74% |
benzyl alcohol
Conditions | Yield |
---|---|
With water | 100% |
tert-butyldimethyl(phenoxy)silane
(benzyloxy)(tert-butyl)dimethylsilane
benzyl alcohol
Conditions | Yield |
---|---|
With 1,11-bis(3-methyl-3H-imidazolium-1-yl)-3,6,9-trioxaundecane di(methanesulfonate) In methanol at 20℃; for 1.41667h; | 100% |
Conditions | Yield |
---|---|
With diisobutylaluminum borohydride In tetrahydrofuran at 25℃; for 1h; Inert atmosphere; | 99% |
Stage #1: benzoic acid With borane-2-methyltetrahydrofuran complex In 2-methyltetrahydrofuran at 0 - 20℃; for 3h; Stage #2: With water In 2-methyltetrahydrofuran Product distribution / selectivity; | 97.1% |
With [Zn(BH4)2(py)] In tetrahydrofuran for 1.5h; Heating; | 96% |
Conditions | Yield |
---|---|
With C32H36ClNO2P2Ru; potassium tert-butylate; hydrogen In tetrahydrofuran at 120℃; under 38002.6 Torr; for 12h; Autoclave; Green chemistry; | 99% |
With C30H34Cl2N2P2Ru; potassium methanolate; hydrogen In tetrahydrofuran at 100℃; under 38002.6 - 76005.1 Torr; for 15h; Glovebox; Autoclave; | 95% |
With lithium aluminium tetrahydride In diethyl ether for 1h; Heating; Yield given; |
Conditions | Yield |
---|---|
With [Ru(2-(methylthio)-N-[(pyridin-2-yl)methyl]ethan-1-amine)(triphenylphosphine)Cl2]; potassium tert-butylate; hydrogen In toluene at 80℃; under 30003 Torr; for 3h; | 99% |
With methanol; sodium methylate at 60℃; Reagent/catalyst; | 99% |
With Ximenia american In water at 30℃; for 72h; pH=5; Enzymatic reaction; | 98% |
(benzyloxy)(tert-butyl)dimethylsilane
benzyl alcohol
Conditions | Yield |
---|---|
With C24H20O3; tetrabutyl ammonium fluoride In tetrahydrofuran at 20℃; for 1h; | 99% |
With water; aluminium In hexane for 15h; Ambient temperature; | 98% |
With polymer-supported dicyanoketene acetal; water In acetonitrile at 20℃; for 24h; Hydrolysis; | 98% |
N,N-diisopropyl benzamide
benzyl alcohol
Conditions | Yield |
---|---|
With n-butyllithium; borane-THF; 2,3-dihydropyrrole at 65℃; | 99% |
With LiPyrrBH3 In tetrahydrofuran at 25℃; for 2h; | 99% |
benzyl tert-butyldiphenylsilyl ether
benzyl alcohol
Conditions | Yield |
---|---|
With potassium fluoride; Tetraethylene glycol at 80℃; for 3.5h; | 99% |
With hafnium tetrakis(trifluoromethanesulfonate) In methanol at 20℃; for 3h; chemoselective reaction; | 97% |
With hafnium tetrakis(trifluoromethanesulfonate) In methanol at 20℃; for 3h; chemoselective reaction; | 97% |
Conditions | Yield |
---|---|
With dimethylsulfide borane complex In 2-methyltetrahydrofuran at 90℃; under 7500.75 Torr; for 0.333333h; Inert atmosphere; Flow reactor; chemoselective reaction; | 99% |
With sodium tetrahydroborate; C36H30F6N10Ni4O10(2+)*2C2F3O2(1-); zinc(II) chloride In tetrahydrofuran at 45℃; for 12h; | 90% |
With methylsilane; potassium tert-butylate In tetrahydrofuran at 70℃; for 72h; Reagent/catalyst; Time; Inert atmosphere; Schlenk technique; Glovebox; chemoselective reaction; | 76% |
Conditions | Yield |
---|---|
zeolite HSZ-360 In neat (no solvent) at 25℃; for 5h; | 100% |
With high p-toluenesulfonate content diphenylamine and terephthalaldehyde resin In acetonitrile at 20℃; for 1h; | 100% |
With monoaluminum phosphate for 0.25h; Product distribution; Heating; other catalyst: AlPO4-Al2O3, other alcohols and phenols; | 99% |
Conditions | Yield |
---|---|
With dichloro-[1,3-bis(4-tert-butylbenzyl)perhydrobenzimidazol-2-ylidene](p-cymene)ruthenium(II); potassium tert-butylate at 120℃; for 24h; Reagent/catalyst; Inert atmosphere; Schlenk technique; Sealed tube; | 100% |
With potassium tert-butylate; copper diacetate In 1,4-dioxane at 130℃; for 24h; | 99% |
With potassium tert-butylate; copper diacetate In 1,4-dioxane at 130℃; for 24h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With N,N-bis[2-oxo-3-oxazolidinyl]phosphorodiamidic chloride In dichloromethane for 1h; Ambient temperature; | 100% |
With N,N'-dimethylaminopyridine; di-tert-butyl dicarbonate In nitromethane at 50℃; for 16h; | 81% |
With boric acid; glycerol Entfernen des entstehenden H2O; |
Conditions | Yield |
---|---|
In pyridine; benzene at 100℃; for 2h; | 100% |
With 1-hydro-3-(3-sulfopropyl)-imidazolium 4-methyl-benzenesulfonate at 60℃; Heating; | 95% |
In pyridine; benzene at 100℃; for 2h; | 84% |
Conditions | Yield |
---|---|
With iodine for 15h; Ambient temperature; | 100% |
With magnesium(II) perchlorate at 20℃; for 0.25h; | 100% |
With nickel dichloride for 0.116667h; microwave irradiation; | 100% |
Conditions | Yield |
---|---|
[Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In toluene for 6h; Heating; | 100% |
With rhizopus niveus lipase; Pseudomonas sp. lipoprotein lipase; Candida antarctica lipase B immobilized on acrylic resin; Carica papaya protease In toluene at 40℃; for 48h; Enzymatic reaction; | 98% |
1-chloro-3-hydroxy-1,1,3,3-tetrabutyldistannoxane In toluene for 16h; Heating; | 96% |
Conditions | Yield |
---|---|
With bifunctional polymer In toluene at 20℃; for 6h; | 100% |
Stage #1: benzoyl chloride; benzyl alcohol In dichloromethane at 20℃; Stage #2: With poly{trans-bicyclo[2.2.1]hept-5-ene-2,3-di(chlorocarbonyl)} In dichloromethane Heating; | 95% |
With triethylamine | 94% |
Conditions | Yield |
---|---|
With chloro(η5-pentamethylcyclopentadienyl)(L-prolinato)iridium(III) In toluene at 95℃; for 24h; Inert atmosphere; Sealed tube; | 100% |
With potassium tert-butylate; copper diacetate In 1,4-dioxane at 130℃; for 48h; | 99% |
With potassium tert-butylate; copper diacetate In 1,4-dioxane at 130℃; for 48h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With dmap In dichloromethane at 20℃; for 96h; Inert atmosphere; | 100% |
With dmap In dichloromethane at 20℃; for 24h; | 92% |
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 1h; Inert atmosphere; | 82% |
Conditions | Yield |
---|---|
zirconium(IV) oxide In toluene for 1h; Heating; in vapor-phase at 150 deg C; | 100% |
LaY zeolite at 116℃; for 8h; Acetylation; | 99% |
With bismuth(lll) trifluoromethanesulfonate at 20℃; for 0.25h; | 99% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene at 120℃; for 24h; | 100% |
With toluene-4-sulfonic acid In benzene at 120℃; for 24h; Inert atmosphere; | 100% |
With toluene-4-sulfonic acid In benzene at 120℃; for 24h; | 100% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0℃; for 1h; | 100% |
With pyridine In acetonitrile 1.) 0 deg C, 1 h, 2.) 25 deg C, 1 h; | 98% |
With sulfuric acid In benzene for 2.5h; Fischer esterification; Heating; | 93% |
Conditions | Yield |
---|---|
With [μN,κP,κC,κN-{2-(i-Pr2PO),6-(CH2NBn)-(C6H3)}Ni]2 In benzene at 50℃; for 1h; | 100% |
With sodium hydroxide In water at 20℃; for 6h; Michael addition; | 99% |
With sodium hydroxide at 20℃; Michael Addition; | 97% |
trichloroacetonitrile
benzyl alcohol
O-benzyl 2,2,2-trichloroacetimidate
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In n-heptane at 0℃; for 0.25h; Solvent; | 100% |
With tetra(n-butyl)ammonium hydrogensulfate; potassium hydroxide In dichloromethane; water at -15 - 20℃; for 1.5h; | 99% |
With potassium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In dichloromethane at -15 - 25℃; for 1h; | 97% |
Conditions | Yield |
---|---|
With C25H27ClIrN4O(1+)*Cl(1-); caesium carbonate at 120℃; for 20h; | 100% |
With potassium tert-butylate; copper diacetate In 1,4-dioxane at 130℃; for 48h; | 99% |
With potassium tert-butylate; copper diacetate In 1,4-dioxane at 130℃; for 48h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 20℃; for 16h; Inert atmosphere; | 100% |
With pyridine In dichloromethane at 23℃; Cooling with ice; Inert atmosphere; | 99% |
With pyridine; dmap In dichloromethane at 0 - 20℃; for 13.5h; | 95% |
Conditions | Yield |
---|---|
With cyanomethylenetributyl-phosphorane In benzene at 100℃; for 24h; | 100% |
With TiO(acac)2 In xylene for 15h; Heating; | 100% |
With fluorosulfonyl fluoride; N-ethyl-N,N-diisopropylamine In 1,2-dichloro-ethane at 20℃; for 5h; | 99% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 100% |
With samarium In acetonitrile at 70℃; for 0.0333333h; | 92% |
With triethylamine In dichloromethane at 20℃; for 12h; | 70.1% |
Conditions | Yield |
---|---|
erbium(III) triflate In acetonitrile at 20℃; for 0.166667h; | 100% |
With erbium(III) chloride for 2h; Heating; | 99% |
In diethyl ether at 0℃; for 2h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
toluene-4-sulfonic acid In toluene for 18h; Heating / reflux; | 100% |
With hydrogenchloride In xylene for 12h; Esterification; Heating; | 95% |
at 160 - 165℃; | |
With hydrogenchloride; xylene |
Conditions | Yield |
---|---|
With 1,3-bis(3,5-bis(trifluoro-ethyl)phenyl)thiourea; 4-pyrrolidin-1-ylpyridine In octane for 24h; Reflux; | 100% |
With dilithium tetra(tert-butyl)zincate at 0℃; for 1h; Temperature; Inert atmosphere; | 100% |
With lanthanum(III) isopropoxide; 2-(2-methoxyethoxy)ethyl alcohol In hexane Reflux; chemoselective reaction; | 97% |
isocyanate de chlorosulfonyle
benzyl alcohol
benzyl N-chlorosulfonylcarbamate
Conditions | Yield |
---|---|
In dichloromethane for 1h; | 100% |
In diethyl ether at 23℃; Inert atmosphere; Cooling with ice; | 97% |
In dichloromethane at -10℃; for 1h; | 69% |
Conditions | Yield |
---|---|
methyltrioxorhenium(VII) for 48h; Ambient temperature; | 100% |
With boron trifluoride diethyl etherate In toluene at 100℃; for 7h; Concentration; Solvent; Time; | 98% |
With trimethylsilyl bromide at 50℃; for 24h; Sealed tube; | 98% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In water; benzene for 22h; Heating; | 100% |
With porous phenol sulfonic acid-formaldehyde resin In neat (no solvent) at 90℃; for 6h; | 91% |
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 2.5h; | 85% |
Conditions | Yield |
---|---|
With [Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In various solvent(s) at 150℃; for 10h; | 100% |
With [bis(acetoxy)iodo]benzene; triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 25℃; for 16h; Mitsunobu reaction; | 100% |
Stage #1: 4-nitro-benzoic acid With N-chlorobenzotriazole; triphenylphosphine In dichloromethane for 0.25h; Cooling; Stage #2: benzyl alcohol With triethylamine In dichloromethane at 20℃; for 0.333333h; | 98% |
Conditions | Yield |
---|---|
With copper(ll) bromide at 175℃; for 8h; Reagent/catalyst; | 100% |
With (NH4)2.8H0.9[ε-VMo9.4V2.6O40Bi2]·7.2H2O at 129.84℃; for 3h; Catalytic behavior; Reagent/catalyst; | 97% |
With benzyl bromide In neat (no solvent) at 120℃; for 24h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; Sealed tube; Green chemistry; | 97% |
Conditions | Yield |
---|---|
With 1,1,1,2,2,2-hexamethyldisilane; pyridinium hydrobromide perbromide In chloroform at 25℃; for 0.5h; | 100% |
With phosphorus tribromide In benzene at 20℃; | 100% |
Stage #1: benzyl alcohol With 1,2,3-Benzotriazole; thionyl chloride In dichloromethane for 0.0833333h; Stage #2: With potassium bromide In dichloromethane; N,N-dimethyl-formamide for 0.5h; | 99% |
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