Dayang Chem (Hangzhou) Co.,Ltd.
DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:103-65-1
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryHangzhou Think Chemical Co. Ltd
Propylbenzene CAS No.:103-65-1 Name: Propylbenzene Synonyms: n-Propylbenzene Molecular Structure Molecular Formula: C9H12 Molecular Weight: 120.19
Cas:103-65-1
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Other
inquiryHenan Sinotech Import&Export Corporation
Product name N-PROPYLBENZENE Synonyms 1-PHENYLPROPANE;PROPYLBENZENE;N-PROPYLBENZENE;1-Propylbenzene;benzene,propyl-;Isocumene;propylbenzene solution;Phenylpropane Cas
Lonwin Chemical Group Limited
N-Propylbenzene CAS：103-65-1 Specification Product name N-PROPYLBENZENE Synonyms 1-PHENYLPROPANE;PROPYLBENZENE;N-PROPYLBENZENE;1-Propylbenzene;benzene,propyl-;Isocumene;propylbenzene solution;Phenylpropane
Cas:103-65-1
Min.Order:1 Kilogram
FOB Price: $100.0 / 150.0
Type:Other
inquiryHangzhou Keyingchem Co.,Ltd
Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
Cas:103-65-1
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
inquiryHangzhou J&H Chemical Co., Ltd.
J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Siwei Development Group Ltd.
Product name: N-Propylbenzene CAS No.：103-65-1 Molecule Formula：C9H12 Molecule Weight：120.19 Purity: 99.0% Package: 25kg/drum Description： Colorless transparent liquid Manufacture Standards：Enterprise Standard TEST
Cas:103-65-1
Min.Order:1 Kilogram
Negotiable
Type:Trading Company
inquiryKono Chem Co.,Ltd
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
Henan Allgreen Chemical Co.,Ltd
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Aecochem Corp.
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Zhuozhou Wenxi import and Export Co., Ltd
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:103-65-1
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAntimex Chemical Limied
Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
Xiamen AmoyChem Co.,Ltd
Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
Hangzhou ZeErRui Chemical Co., Ltd.
Known for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers. Prompt reaction, good quality and best service make us reliable and outstanding in this industry.Appearance:Clear slightly yellow liqui
Cas:103-65-1
Min.Order:0
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Type:Lab/Research institutions
inquiryAmadis Chemical Co., Ltd.
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:103-65-1
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryHENAN SUNLAKE ENTERPRISE CORPORATION
N-PROPYLBENZENE Basic information Product Name: N-PROPYLBENZENE Synonyms: 1-PHENYLPROPANE;PROPYLBENZENE;N-PROPYLBENZENE;1-Propylbenzene;benzene,propyl-;Isocumene;Phenylpropane;propyl-benzen
Hebei Ruishun Trade Co.,Ltd
Hebei ruishun trade co.,ltd, registered capital one million,have a production of pharmaceutical raw materials, pharmaceutical raw materials factory reagent r&d center,seek development by credit reputation.our products have a large price advanta
Hangzhou Share Chemical Co., Ltd
At Share Chemical Company, we scrupulously abide by our policy of “Excellent Quality at a Reasonable Price”. We strive to satisfy all of our customers by providing the finest quality products supported by the finest in customer servi
Shanghai united Scientific Co.,Ltd.
United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
Hangzhou Yierdechem Co. Ltd
With about ten years experiences in the field of pharmaceutical chemicals, Yierdechem has established solid business cooperation relationships with many large companys worldwide.As a leading supplier of API and pharmaceutical intermediates, holds its
Capot Chemical Co., Ltd.
At Capot,We can synthesize and purify your complex molecules from 100 gram to 10 tons.Appearance:Clear colorless to light yellow liquid Storage:Dry,Seal and Cool place Package:1G,5G,10G,25G,100G,250G,500G,1KG,5KG,10KG,25KG,50KG,100KG,150KG,200KG. App
Shanghai Run-Biotech Co., Ltd.
Shanghai, Run-Biotech Co., Ltd is a leading domestic pharmaceutical, biopharmaceutical, and health care products R & D outsourcing services company. As an innovation-driven and customer-focused company, Run Biotech provides a broad and integrated por
Kunshan Yalong Trading Co,.Ltd
1.High quality 2. Free sample available 3. Competitive price 4.Experienced service team 5.Fast delivery 6. Considerate after-sale serviceAppearance:Colorless or light yellow liquid Package:as per clients' request Application:In organic synthesis. Cel
Cas:103-65-1
Min.Order:0
Negotiable
Type:Trading Company
inquiryHangZhou Yaos COOP IMP.&EXP CO. LTD
hangzhou yaos coop. superiority 1.high quality and competetive price 1)for azo initiators exported we can offer coa certificate and official invoice. 2)we are manufacturer with own factory, can provide high quality products with factory pri
Wuxi Morality Chemical Co., Ltd
Do best quality products, erect the morality model Application:please email us, thanks
Hangzhou Fenjun Chemical Co Ltd.
Hangzhou Keying Chem Co., Ltd. Is a comprehensive enterprise, dedicated to the development, production and marketing of chemicals. As a technology innovative and service professional enterprise, Our company mainly engages in global pharmaceutical, ch
Debye Scientific
Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
Sparrow Chemical Co.,Ltd
Our company provides the best service for our customers. Under the premise of ensuring quality and delivery date, give customers the best price. The company is more willing to meet our customers. If you want to visit our factories and warehouses, we
Synthetic route
| Conditions | Yield |
|---|---|
| With Pt-Sn-citrate; hydrogen In methanol at 50℃; under 3800 Torr; for 3h; var. temperatures; var. pressures; | 100% |
| With Pt-Sn-citrate; hydrogen In methanol at 50℃; under 3800 Torr; for 3h; | 100% |
| With C49H60BF2IrN5(1+)*C32H12BF24(1-); hydrogen In 1,2-dichloro-ethane at 20℃; for 0.166667h; Reagent/catalyst; Schlenk technique; | 100% |
| Conditions | Yield |
|---|---|
| With C28H18Co(1-)*K(1+)*2C4H10O2; hydrogen In toluene at 60℃; under 1500.15 Torr; for 24h; Temperature; Time; Reagent/catalyst; chemoselective reaction; | 100% |
| With iron(III) chloride; lithium aluminium tetrahydride; hydrogen In tetrahydrofuran at 18℃; under 750.075 Torr; for 20h; Inert atmosphere; Sealed tube; | 100% |
| In methanol for 0.5h; UV-irradiation; | 99% |
| Conditions | Yield |
|---|---|
| With hydrogen In ethanol at 39.84℃; under 760.051 Torr; for 5h; | 100% |
| With hydrogen In 1,4-dioxane at 200℃; under 15001.5 Torr; | 95.8% |
| Stage #1: 1-phenyl-propan-1-one With iron(III) chloride In methanol at 20℃; for 0.05h; Stage #2: In methanol at 20℃; for 0.166667h; chemoselective reaction; | 91% |
| Conditions | Yield |
|---|---|
| With hydrogen; sodium triethylborohydride In tetrahydrofuran under 30003 Torr; for 20h; Catalytic behavior; Inert atmosphere; | 100% |
| With water; zinc; chloro(1,5-cyclooctadiene)rhodium(I) dimer In 1,4-dioxane at 90℃; for 20h; | 99% |
| With [Fe(nacnac)dippCH2SiMe3]; N-butylamine; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane In benzene-d6 at 20℃; for 16h; Sealed tube; Schlenk technique; Glovebox; Inert atmosphere; | 99% |
-
-
3277-26-7
1,1,3,3-Tetramethyldisiloxane
-
-
70110-65-5
2-phenoxy-1-phenylpropane-1, 3-diol
-
-
103-65-1
Propylbenzene
| Conditions | Yield |
|---|---|
| With tris(pentafluorophenyl)borate; water In dichloromethane at 20℃; for 16h; Inert atmosphere; | 100% |
| Conditions | Yield |
|---|---|
| With chloro-trimethyl-silane; acetonitrile; sodium iodide In hexane for 24h; Ambient temperature; | 99% |
| With chloro-trimethyl-silane; acetonitrile; sodium iodide In hexane for 24h; Ambient temperature; | 99% |
| With hydrogen In ethanol at 80℃; under 2250.23 Torr; for 3h; Catalytic behavior; Temperature; Solvent; Inert atmosphere; | 94% |
| Conditions | Yield |
|---|---|
| With LiCrH4*2LiCl*2THF In tetrahydrofuran at 25℃; for 12h; | 99% |
| With indium(III) chloride; sodium tetrahydroborate In acetonitrile at 20℃; for 2h; | 95% |
| With sodium tetrahydroborate; water In methanol at 20℃; for 0.5h; | 87% |
-
-
993-07-7
trimethylsilan
-
A
-
104-53-0
3-phenyl-propionaldehyde
-
D
-
103-65-1
Propylbenzene
-
E
-
14629-60-8
trimethyl(3-phenylpropoxy)silane
| Conditions | Yield |
|---|---|
| In benzene-d6 react. of Fe complex and HSiMe3 in benzene, 90°C, 9 h; yields detd. by (1)H-NMR (C5H5Fe(CO)H(SiMe3)2; elem. anal.) and GL-chromy. (other products); | A 0% B 91% C 10% D 0% E 98% |
| Conditions | Yield |
|---|---|
| With hydrogen In methanol at 30℃; under 760.051 Torr; for 2h; | A 97% B 3% |
| With hydrogen; poly(amidoamine) dendron-stabilised Pd(0) nanoparticle In dichloromethane at 25℃; under 760.051 Torr; for 1h; | A 96% B 4% |
| With hydrogen; Et4N In 1,2-dimethoxyethane at 100℃; under 38000 Torr; for 18h; Product distribution; further unsaturated compounds of different types; | A 8% B 90% |
-
-
103-65-1
Propylbenzene
| Conditions | Yield |
|---|---|
| With samarium diiodide In tetrahydrofuran at 67℃; Irradiation; | 97% |
| Conditions | Yield |
|---|---|
| With palladium dichloride In methanol at 40℃; for 18h; Inert atmosphere; Green chemistry; chemoselective reaction; | 96% |
| With [IrCl(CO)(PPh3)2]; hydrazine hydrate; potassium hydroxide In methanol at 160℃; for 3h; Wolff-Kishner Reduction; Sealed tube; | 81% |
| With [IrCl(CO)(PPh3)2]; hydrazine hydrate; potassium hydroxide In methanol at 160℃; for 3h; Sealed tube; | 81% |
| Conditions | Yield |
|---|---|
| With potassium hydroxide; hydrogen; Aliquat 336; palladium on activated charcoal In 2,2,4-trimethylpentane at 50℃; for 0.833333h; Product distribution; various time, solvents; also in the presence of various aromatic halides as promoters; further benzylic alcohols; | A 96% B 4% |
-
-
1631-73-8
trimethylstannane
-
A
-
104-53-0
3-phenyl-propionaldehyde
-
C
-
122-97-4
3-Phenyl-1-propanol
-
D
-
103-65-1
Propylbenzene
| Conditions | Yield |
|---|---|
| In benzene-d6 react. of Fe complex and HSnMe3 in benzene, 120°C, 7 h; yields detd. by (1)H-NMR (C5H5Fe(CO)H(SnMe3)2; elem. anal.) and GL-chromy. (other products); | A <3 B 73% C 96% D 0% |
| In benzene-d6 Irradiation (UV/VIS); irradn. of Fe complex and HSnMe3 in benzene for 6 h; yields detd. by (1)H-NMR and GL-chromy.; | A 79% B 82% C 0% D 0% |
| Conditions | Yield |
|---|---|
| With tetrahydroxydiboron; palladium 10% on activated carbon; water In dichloromethane at 20℃; for 5h; Inert atmosphere; | 95% |
| With 2C2H3O2(1-)*Pd(2+)*3Na(1+)*C18H12O9PS3(3-); hydrogen; glycerol at 100℃; under 2250.23 Torr; for 2h; Schlenk technique; | 92% |
| With hydrogen; palladium on activated charcoal In hexane under 1520 Torr; Thermodynamic data; ΔH; |
-
-
3647-71-0
N-benzyl-2-phenylethylamine
-
-
97-93-8
triethylaluminum
-
A
-
103-65-1
Propylbenzene
-
B
-
64-04-0
phenethylamine
-
C
-
103-29-7
1,1'-(1,2-ethanediyl)bisbenzene
-
D
-
108-88-3
toluene
| Conditions | Yield |
|---|---|
| In benzene for 38h; Irradiation; | A 50% B 95% C n/a D 14% |
-
-
106-94-5
propyl bromide
-
-
603-35-0
triphenylphosphine
-
A
-
103-65-1
Propylbenzene
-
B
-
7650-84-2
diphenylphosphinopropane
| Conditions | Yield |
|---|---|
| Stage #1: triphenylphosphine With lithium In diethyl ether at 20℃; for 3h; Inert atmosphere; Stage #2: propyl bromide In diethyl ether at 0 - 30℃; for 2.5h; | A 94.8% B 92.4% |
| Stage #1: triphenylphosphine With lithium In diethyl ether at 20℃; for 3h; Inert atmosphere; Stage #2: propyl bromide In diethyl ether at 0 - 30℃; for 1.5h; Inert atmosphere; |
| Conditions | Yield |
|---|---|
| With triethylsilane; tris(pentafluorophenyl)borate In dichloromethane at 20℃; | 94% |
| With triethylsilane; tris(pentafluorophenyl)borate In dichloromethane at 20℃; for 20h; | 94% |
| With 1,1,3,3-Tetramethyldisiloxane; tris(pentafluorophenyl)borate In benzene-d6 at 23℃; for 1h; Glovebox; Schlenk technique; | 100 %Spectr. |
-
-
1631-73-8
trimethylstannane
-
A
-
104-53-0
3-phenyl-propionaldehyde
-
C
-
122-97-4
3-Phenyl-1-propanol
-
D
-
103-65-1
Propylbenzene
| Conditions | Yield |
|---|---|
| In benzene-d6 react. of Fe complex and HSnMe3 in benzene, 60°C, 13 h; yields detd. by (1)H-NMR (C5H5Fe(CO)H(SnMe3)2; elem. anal.) and GL-chromy. (other products); | A 0% B 88% C 94% D <3 |
| In benzene-d6 Irradiation (UV/VIS); irradn. of Fe complex and HSnMe3 in benzene for 7 h; yields detd. by (1)H-NMR and GL-chromy.; | A 0% B 85% C <3 D 86% |
| Conditions | Yield |
|---|---|
| With C41H38BFeN3P2; hydrogen In tetrahydrofuran at 20 - 90℃; under 7500.75 Torr; for 27h; Inert atmosphere; | A 94% B 11% |
| With formic acid; para-xylene; 1,3-bis(2,4,6-trimethylphenyl)-3,4,5,6-tetrahydro-pyrimidin-1-ium palladium (divinyltetramethyldisiloxane); triethylamine In acetonitrile at 80℃; for 2h; Catalytic behavior; Inert atmosphere; Schlenk technique; Reflux; chemoselective reaction; | |
| With C42H44ClN4P2Ru(1+)*Cl(1-); potassium tert-butylate; isopropyl alcohol at 80℃; for 72h; Schlenk technique; Inert atmosphere; | A n/a B 77 %Spectr. |
| With hydrogen; iron(II) acetate; diisobutylaluminium hydride In tetrahydrofuran; toluene at 30℃; under 1500.15 Torr; for 3h; stereoselective reaction; | A n/a B n/a |
-
-
540-54-5
1-Chloropropane
-
-
603-35-0
triphenylphosphine
-
A
-
103-65-1
Propylbenzene
-
B
-
7650-84-2
diphenylphosphinopropane
| Conditions | Yield |
|---|---|
| Stage #1: triphenylphosphine With lithium In tetrahydrofuran at 20℃; for 3h; Inert atmosphere; Stage #2: 1-Chloropropane In tetrahydrofuran at 5 - 50℃; for 6.25h; | A 93.5% B 91.6% |
-
-
21040-45-9
Cinnamyl acetate
-
-
103-65-1
Propylbenzene
| Conditions | Yield |
|---|---|
| With sodium tetrahydroborate; nickel dichloride In methanol at -20℃; for 0.5h; | 93% |
| Conditions | Yield |
|---|---|
| With sodium tetrahydroborate; 2,2'-azobis(isobutyronitrile); polystyrene-supported organotin catalyst In N,N-dimethyl acetamide at 80℃; for 6.5h; | 93% |
| With indium(III) chloride; sodium tetrahydroborate In acetonitrile at 20℃; for 2h; | 90% |
| With triethylsilane; indium(III) chloride; triethyl borane In hexane; dichloromethane at 20℃; for 2h; | 83% |
| Multi-step reaction with 2 steps 1: tetrahydrofuran / 0.5 h / 20 °C / Glovebox; Sealed tube; Irradiation 2: sodium methylate / 12 h / 20 °C / Glovebox; Sealed tube; Irradiation View Scheme |
| Conditions | Yield |
|---|---|
| With hydrogen; sodium triethylborohydride In tetrahydrofuran at 23℃; under 30003 Torr; for 20h; Reagent/catalyst; Autoclave; | 92% |
| With hydrogen; sodium triethylborohydride In tetrahydrofuran at 23℃; under 30402 Torr; for 70h; Catalytic behavior; Inert atmosphere; Schlenk technique; | 36% |
| With hydrogen; sodium triethylborohydride In tetrahydrofuran at 23℃; under 30402 Torr; for 18h; Reagent/catalyst; Glovebox; Inert atmosphere; | 12% |
| Conditions | Yield |
|---|---|
| With formic acid; palladium on activated charcoal In ethanol; benzene for 0.166667h; Heating; Yields of byproduct given; | A n/a B 92% |
| With formic acid; palladium on activated charcoal In ethanol; benzene for 0.0833333h; Heating; Yield given. Yields of byproduct given; |
| Conditions | Yield |
|---|---|
| With sodium tetrahydroborate; water In methanol at 20℃; for 0.166667h; | 92% |
| Conditions | Yield |
|---|---|
| (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride In tetrahydrofuran at -78 - 67℃; | 91% |
-
-
1631-73-8
trimethylstannane
-
A
-
104-53-0
3-phenyl-propionaldehyde
-
C
-
122-97-4
3-Phenyl-1-propanol
-
D
-
103-65-1
Propylbenzene
| Conditions | Yield |
|---|---|
| In benzene-d6 react. of Fe complex and HSnMe3 in benzene, 120°C, 6 h; yields detd. by (1)H-NMR and GL-chromy.; | A <3 B 91% C 91% D <3 |
| In benzene-d6 Irradiation (UV/VIS); irradn. of Fe complex and HSnMe3 in benzene for 24 h; yields detd. by (1)H-NMR and GL-chromy.; | A 0% B 0% C <3 D 37% |
| Conditions | Yield |
|---|---|
| With sodium tetrahydroborate; water In methanol at 20℃; for 0.25h; | 91% |
| Conditions | Yield |
|---|---|
| With sodium tetrahydroborate; aluminium trichloride In tetrahydrofuran for 2h; Heating; | A 90% B 7 % Chromat. |
| With sodium tetrahydroborate; aluminium trichloride In tetrahydrofuran for 2h; Ambient temperature; Yield given. Yields of byproduct given; | |
| With hydrogen In toluene at 80℃; under 15001.5 Torr; for 24h; Autoclave; chemoselective reaction; | |
| With hydrogen In tetrahydrofuran at 50℃; under 15001.5 Torr; for 24h; Autoclave; chemoselective reaction; |
| Conditions | Yield |
|---|---|
| With Ti8O8(14+)*6C8H4O4(2-)*4O(2-)*3.3Li(1+)*0.7Co(2+)*0.7C4H8O*0.7H(1-); hydrogen In neat (no solvent) at 120℃; under 37503.8 Torr; for 18h; | 100% |
| With nickel at 220 - 240℃; under 73550.8 Torr; Hydrogenation; | |
| With platinum(IV) oxide; acetic acid Hydrogenation; |
-
-
103-65-1
Propylbenzene
-
-
115499-97-3
4-(methoxymethoxy)-4'-methoxybenzophenone
-
-
671791-56-3
1-(4-methoxymethoxyphenyl)-1-(4-methoxyphenyl)-2-phenylbutan-1-ol
| Conditions | Yield |
|---|---|
| Stage #1: phenylpropane With n-butyllithium; N,N,N,N,-tetramethylethylenediamine; potassium tert-butylate In tetrahydrofuran; hexane at 20℃; for 0.5h; Stage #2: 4-(methoxymethoxy)-4'-methoxybenzophenone In tetrahydrofuran; hexane at -78 - 20℃; for 4.5h; | 97% |
| Stage #1: phenylpropane With n-butyllithium; N,N,N,N,-tetramethylethylenediamine; potassium tert-butylate Stage #2: 4-(methoxymethoxy)-4'-methoxybenzophenone | 97% |
-
-
103-65-1
Propylbenzene
-
-
24503-35-3
2,4-dinitro-1-propylbenzene
| Conditions | Yield |
|---|---|
| With nitric acid; Chloroacetic anhydride at 50℃; for 4h; | 96% |
| With sulfuric acid; nitric acid at 0 - 20℃; | 89% |
| With sulfuric acid; nitric acid | |
| With sulfuric acid; nitric acid | |
| With sulfuric acid; nitric acid at 0 - 20℃; for 0.5h; |
-
-
88-67-5
2-Iodobenzoic acid
-
-
103-65-1
Propylbenzene
-
-
1427465-30-2
1-(4-propylphenyl)-1H-1λ3-benzo[b]iodo-3(2H)-one
| Conditions | Yield |
|---|---|
| Stage #1: 2-Iodobenzoic acid With Oxone; sulfuric acid at 5 - 20℃; for 0.5h; Stage #2: phenylpropane In dichloromethane at 5 - 20℃; for 3h; | 94% |
| Conditions | Yield |
|---|---|
| With C20H24B10Cl4FeN6; dihydrogen peroxide In methanol at 20℃; for 6h; | 93% |
| With lithium aluminium tetrahydride; 2,2'-azobis(isobutyronitrile); oxygen Kinetics; relative chain propagation rates; | |
| With NADPH In dimethyl sulfoxide at 30℃; pH=7.4; Product distribution; Further Variations:; Reagents; | 99 % Chromat. |
| Conditions | Yield |
|---|---|
| With potassium permanganate; Rexyn 101 H ion exchange resin In dichloromethane for 5.45h; Heating; | 93% |
| With potassium permanganate on Zeolite beta In 1,2-dichloro-ethane for 96h; Ambient temperature; | 92% |
| With sodium bromate; sulfuric acid; silica gel at 20℃; for 3h; | 92% |
| Conditions | Yield |
|---|---|
| With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); water In ethyl acetate at 60℃; for 6h; Wohl-Ziegler Bromination; | 93% |
| With hydrogen bromide; oxygen In water; ethyl acetate at 20℃; for 10h; Irradiation; | 61% |
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