As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
Cas:31087-44-2
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Cas:31087-44-2
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inquiry1. Timely and efficient service to ensure communication with customers 2. Produce products of different specifications and sizes according to your requirements. 3. Quality procedures and standards recognized by SGS. Advanced plant equipment ensures s
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inquiryAppearance:white or light yellow crystalline powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:By
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Cas:31087-44-2
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inquiryJ&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
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
factory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
Cas:31087-44-2
Min.Order:1 Kilogram
FOB Price: $18.0 / 20.0
Type:Trading Company
inquiryShandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W
Cas:31087-44-2
Min.Order:1 Gram
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
Cas:31087-44-2
Min.Order:1 Metric Ton
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Type:Trading Company
inquirySAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in
Cas:31087-44-2
Min.Order:0 Metric Ton
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inquiryHigh quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
We are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
Cas:31087-44-2
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inquiryStock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
Cas:31087-44-2
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Type:Lab/Research institutions
inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
Cas:31087-44-2
Min.Order:100 Gram
Negotiable
Type:Lab/Research institutions
inquiryhigh 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
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
GMP factory Packing with pallet as buyer's special request Best service after shipment with e-mail Cargos together with container sales service available Api, inhibitor, and fine chemicals for more than 6 years. Application:chiral comp
Cas:31087-44-2
Min.Order:0 Metric Ton
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Type:Trading Company
inquiry"HANGZHOU TIANYE CHEMICALS Co.LTD , Located in Eastern Science and Innovation Park Hangzhou .We are a high-tech enterprise specialized in technical research and development, production, development and trade of chemical products. We supply Multiple s
(R)-(-)-2-Pentanol cas 31087-44-2Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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:31087-44-2
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiry(R)-(-)-2-Pentanol Basic information Product Name: (R)-(-)-2-Pentanol Synonyms: (R)-(-)-2-PENTANOL;(R)-2-PENTANOL;(R)-(-)-2-HYDROXYPENTANE;(-)(R)-pentanol-(2);(R)-p
Changzhou Extraordinary Pharmatech co., LTD. As a leading chemical manufacturer and supplier in China.DAS authentication is passed.We can provide the popular precursor chemicals, we have our own strong R & D team, have our own laboratories and fa
Cas:31087-44-2
Min.Order:1 Gram
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Type:Lab/Research institutions
inquiryPrice, service, company and transport advantage: 1. Best service, place of origin China, high quality, and reasonable price. 2. It's customers' right to choose the package (EMS, DHL, FEDEX, UPS). 3. It's customers' right
Cas:31087-44-2
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Type:Trading Company
inquiry2-Pentanone
(R)-2-pentanol
Conditions | Yield |
---|---|
With hydrogen; C19H29B10ClNORh In ethanol at 80℃; under 760.051 Torr; for 1h; | 92% |
With glucose dehydrogenase; ketoreductase Kred-107; glucose; NADPH for 24h; Enzymatic reaction; optical yield given as %ee; stereoselective reaction; | 89% |
With Leifsonia sp. S749 cells alcohol dehydrogenase; nicotinamide adenine dinucleotide; isopropyl alcohol In phosphate buffer at 25℃; for 24h; pH=7.0; | 17% |
Conditions | Yield |
---|---|
SADH from Thermoanaerobacter ethanolicus at 37℃; Product distribution; enantiospecificity in enzymatic reaction; var. temp.; | |
With secondary alcohol dehydrogenase of Thermoanaerobacter ethanolicus,Tris buffer; NADP In isopropyl alcohol at 37℃; for 10h; Rate constant; Product distribution; different coenzymes: effect of the coenzyme on the enantioselectivity of alcohol dehydrogenase; other temp.; | |
With mercaptoethyl alcohol; Tris-HCl buffer; alcohol dehydrogenase from Thermoanaerobium brockii; NADP; isopropyl alcohol In water at 22℃; for 5h; Mechanism; various buffers; effect of pH, reaction time, temperature, concentration of substrate and of 2-propanol; also with growing cells; also with enzyme immobilized on different supports: effect of contact time and of concentration of NADP; |
(R)-2-pentanol
Conditions | Yield |
---|---|
With potassium hydroxide In methanol at 50℃; for 0.5h; |
Conditions | Yield |
---|---|
With lyophilized cells of Rhodococcus ruber DSM 44541; acetone In phosphate buffer at 24℃; for 24h; pH=8.0; Enzyme kinetics; | |
With lyophilized cells of Rhodococcus ruber DSM 44541; acetone In phosphate buffer at 24℃; for 24h; pH=8.0; Title compound not separated from byproducts.; | |
Stage #1: (+/-)-2-pentanol With potassium bromide In water at 25℃; for 0.166667h; Resolution of racemate; Stage #2: With [bis(acetoxy)iodo]benzene In water at 25℃; for 2h; enantioselective reaction; | A n/a B n/a |
With wild type flavoprotein alcohol oxidase from Phanerochaete chrysosporium In aq. phosphate buffer at 35℃; for 24h; pH=7.5; Kinetics; enantioselective reaction; | A n/a B n/a |
vinyl acetate
(+/-)-2-pentanol
A
(S)-2-pentanol
B
(R)-2-pentanol
C
(R)-pentan-2-yl acetate
Conditions | Yield |
---|---|
With Escherichia coli BioH In hexane at 35℃; for 28h; Resolution of racemate; optical yield given as %ee; enantioselective reaction; | |
With immobilized LipG9 In hexane at 35℃; for 24h; Solvent; Temperature; Resolution of racemate; Enzymatic reaction; | A n/a B n/a C n/a D n/a |
(R)-benzoic acid 1-methylbutyl ester
(R)-2-pentanol
Conditions | Yield |
---|---|
With potassium hydroxide In tetrahydrofuran; methanol; water at 25℃; for 2h; | 93.5% |
(R)-2-pentanol
Conditions | Yield |
---|---|
With water; sodium hydroxide at 41 - 75℃; for 17.5h; Temperature; |
Conditions | Yield |
---|---|
With water; sodium hydroxide at 41 - 75℃; for 17.5h; |
Conditions | Yield |
---|---|
With Candida antarctica lipase B wild-type (WT); water In aq. phosphate buffer; acetonitrile at 37℃; for 5h; pH=7.5; Reagent/catalyst; Resolution of racemate; enantioselective reaction; | A 40% B n/a |
With phosphate buffer; immobilized lipase PS In methanol at 30℃; pH=7.0; | |
With Candida antarctica lipase B immobilized on acrylic resin catalyst at 20 - 25℃; for 8h; pH=7.4; aq. phosphate buffer; Enzymatic reaction; optical yield given as %ee; enantioselective reaction; |
Conditions | Yield |
---|---|
With water; sodium hydrogencarbonate at 37℃; pH=8 - 8.5; Reagent/catalyst; Time; Green chemistry; Enzymatic reaction; |
Conditions | Yield |
---|---|
With 1,4-dihydronicotinamide adenine dinucleotide; PIPES buffer; particulate methane monooxygenase In water at 45℃; pH=7.3; Kinetics; Oxidation; | |
With Durohydroquinone; ammonia monooxygenase of nitrosomonas europaea In aq. phosphate buffer at 30℃; under 760.051 Torr; for 0.166667h; Reagent/catalyst; regioselective reaction; | A n/a B n/a C n/a |
With Durohydroquinone; methylosinus trichosporium OB3b In aq. phosphate buffer at 30℃; under 760.051 Torr; for 0.166667h; Reagent/catalyst; enantioselective reaction; | A n/a B n/a C n/a |
(+/-)-2-pentanol
A
(S)-2-pentanol
B
(R)-2-pentanol
C
2-Pentanone
Conditions | Yield |
---|---|
With whole lyophilised cells of Rhodococcus ruber DSM; acetone In phosphate buffer at 30℃; for 38h; pH=8.0; | |
With [bis(acetoxy)iodo]benzene; potassium bromide; (S,S)-chloro[2,2'-[1,2-cyclohexanediylbis(nitrilomethylidyne)]bis-[4,6-bis(1,1-dimethylethyl)phenolato]](2-)-N,N',O,O'-manganese In dichloromethane at 20℃; for 1h; Product distribution; Kinetics; Further Variations:; Solvents; | |
With [bis(acetoxy)iodo]benzene; potassium bromide In dichloromethane; water at 20℃; for 1h; Title compound not separated from byproducts.; | |
With NADP In acetone at 50℃; for 22h; pH=8; Resolution of racemate; | |
Stage #1: (+/-)-2-pentanol With 36Zn(2+)*6O(2-)*12C40H44O12S4(4-)*12Mn(3+)*12C30H34N2O6(4-)*21H2O*38C3H7NO In dichloromethane; water for 0.0833333h; Resolution of racemate; Stage #2: With [bis(acetoxy)iodo]benzene; tetraethylammonium bromide In dichloromethane; water at 0℃; for 0.5h; Reagent/catalyst; Optical yield = 86 %ee; enantioselective reaction; |
Conditions | Yield |
---|---|
With diphenic acid; (R,R)-1,2-diphenylethylenediamine In ethanol Title compound not separated from byproducts; | |
With C13H14N2*C18H14O8 In water; acetonitrile at 20℃; Resolution of racemate; optical yield given as %ee; enantioselective reaction; | |
With homochiral metal-organic cage [Zn3(deprotonated [3+3] macrocyclic Schiff base of trans-1,2-diaminocyclohexane and 4-tert-butyl-2,6-diformylphenol)2] coated capillary column In dichloromethane at 75℃; Reagent/catalyst; Temperature; Resolution of racemate; enantioselective reaction; |
(+/-)-2-pentanol
(R)-2-pentanol
Conditions | Yield |
---|---|
With sulfuric acid; (3R,4R)-1-phenyl-3,4-dihydroxy-2,5-dioxopyrrolidine und Verseifen des durch Umkrystallisieren aus Isopropylalkohol erhaltenen (+)-Tartranilsaeureesters; | |
With phthalic anhydride Veresterung, Spaltung des sauren Phthalats mit Brucin und Verseifung; | |
ueber N2-<(R)-1-Methyl-butoxycarbonyl>-L-asparagin; |
(1R)-1-Methylbutyl dodecanoate
(R)-2-pentanol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether for 2h; Heating; | 20% |
2-Pentanol 3,5-dinitrobenzoate ester
A
(S)-2-pentanol
B
(R)-2-pentanol
Conditions | Yield |
---|---|
With sodium hydroxide In tetrahydrofuran at 20℃; for 5h; Hydrolysis; |
Pent-3-yn-2-ol
(R)-2-pentanol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: aq. NaOH 2: aq. NaOH / ethanol 3: H2 / PtO2 View Scheme |
phthalic acid mono-((R)-1-methyl-but-2-ynyl) ester
(R)-2-pentanol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aq. NaOH / ethanol 2: H2 / PtO2 View Scheme |
(R)-pent-4-en-2-ol
(R)-2-pentanol
Conditions | Yield |
---|---|
With hydrogen; platinum on activated charcoal |
(+/-)-2-pentanol
(S)-threonyl-(S)-phenylglycine
A
(S)-2-pentanol
B
(R)-2-pentanol
D
C5H12O*C12H16N2O4
Conditions | Yield |
---|---|
for 0.5h; Resolution of racemate; optical yield given as %ee; |
(+/-)-2-pentanol
Octanoic acid
A
(S)-2-pentanol
B
(R)-2-pentanol
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilized on acrylic resin catalyst In pentane at 20 - 25℃; for 24h; Enzymatic reaction; optical yield given as %ee; enantioselective reaction; | A n/a B n/a C 1.4 g |
(+/-)-2-pentanol
acetic acid
A
(S)-2-pentanol
B
(R)-2-pentanol
C
(R)-pentan-2-yl acetate
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilized on acrylic resin catalyst In pentane at 20 - 25℃; for 24h; Enzymatic reaction; optical yield given as %ee; enantioselective reaction; | A n/a B n/a C 0.81 g |
(+/-)-2-pentanol
hexanoic acid
A
(S)-2-pentanol
B
(R)-2-pentanol
C
(R)-2-pentyl hexanoate
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilized on acrylic resin catalyst In pentane at 20 - 25℃; for 24h; Enzymatic reaction; optical yield given as %ee; enantioselective reaction; | A n/a B n/a C 1.21 g |
(+/-)-2-pentanol
butyric acid
A
(S)-2-pentanol
B
(R)-2-pentanol
C
(R)-2-pentyl butanoate
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilized on acrylic resin catalyst In pentane at 20 - 25℃; for 24h; Enzymatic reaction; optical yield given as %ee; enantioselective reaction; | A n/a B n/a C 1.02 g |
(+/-)-2-pentanol
acetic acid
A
(S)-2-pentanol
B
(R)-2-pentanol
C
(R)-pentan-2-yl acetate
Conditions | Yield |
---|---|
With Candida antarctica lipase B catalyst In n-heptane at 20 - 25℃; for 24h; Enzymatic reaction; optical yield given as %ee; enantioselective reaction; |
(+/-)-2-pentanol
hexanoic acid
A
(S)-2-pentanol
B
(R)-2-pentanol
C
(R)-2-pentyl hexanoate
D
(S)-2-pentyl hexanoate
Conditions | Yield |
---|---|
With Candida antarctica lipase B catalyst In n-heptane at 20 - 25℃; for 24h; Enzymatic reaction; optical yield given as %ee; enantioselective reaction; |
Isopropenyl acetate
(+/-)-2-pentanol
A
(S)-2-pentanol
B
(R)-2-pentanol
C
(R)-pentan-2-yl acetate
Conditions | Yield |
---|---|
With immobilized LipG9 In hexane at 35℃; for 24h; Resolution of racemate; Enzymatic reaction; |
(+/-)-2-pentanol
ethyl acetate
A
(S)-2-pentanol
B
(R)-2-pentanol
C
(R)-pentan-2-yl acetate
Conditions | Yield |
---|---|
With immobilized LipG9 In hexane at 35℃; for 24h; Resolution of racemate; Enzymatic reaction; |
(R)-(+)-pent-3-yn-2-ol
(R)-2-pentanol
Conditions | Yield |
---|---|
With hydrogen; platinum(IV) oxide |
(R)-2-pentanol
Conditions | Yield |
---|---|
With diethyl ether; colloid; palladium Hydrogenation; |
5-bromo-2-chloropyridine
(R)-2-pentanol
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran; mineral oil at 80℃; for 1h; Solvent; Temperature; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
Stage #1: (R)-2-pentanol With ethylmagnesium bromide In tetrahydrofuran at 0 - 20℃; for 1.5h; Inert atmosphere; Stage #2: 4,7-dibromo-5,6-bis(bromomethyl)benzo[c][1,2,5]thiadiazole In tetrahydrofuran at 20 - 80℃; for 12.5h; Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
With pyridine; thionyl chloride In toluene | 86% |
(R)-2-pentanol
p-toluenesulfonyl chloride
Conditions | Yield |
---|---|
With pyridine at 0℃; for 3h; | 84% |
(E)-2-methyl-2-pentenoyl chloride
(R)-2-pentanol
(E)-(R)-(1)-1-methylbutyl 2-methyl-2-pentenoate
Conditions | Yield |
---|---|
With pyridine In diethyl ether at 25℃; for 2h; | 77% |
(R)-2-pentanol
(R)-1-fluoroindan-1-carboxylic acid methyl ester
(R)-2-pentyl (R)-1-fluoroindan-1-carboxylate
Conditions | Yield |
---|---|
Stage #1: (R)-2-pentanol With n-butyllithium In tetrahydrofuran; hexane at -5℃; for 0.5h; Inert atmosphere; Stage #2: (R)-1-fluoroindan-1-carboxylic acid methyl ester In tetrahydrofuran; hexane for 0.25h; Inert atmosphere; | 76% |
(R)-2-pentanol
(E)-2,4-Dimethyl-2-pentenoic acid chloride
(R)-(-)-2'-pentyl (E)-2,4-dimethyl-2-pentenoate
Conditions | Yield |
---|---|
With pyridine In diethyl ether at 25℃; for 2h; | 73% |
(R)-2-pentanol
(S)-1-fluoroindan-1-carboxylic acid methyl ester
(R)-2-pentyl (S)-1-fluoroindan-1-carboxylate
Conditions | Yield |
---|---|
Stage #1: (R)-2-pentanol With n-butyllithium In tetrahydrofuran; hexane at -5℃; for 0.5h; Inert atmosphere; Stage #2: (S)-1-fluoroindan-1-carboxylic acid methyl ester In tetrahydrofuran; hexane for 0.25h; Inert atmosphere; | 71% |
Conditions | Yield |
---|---|
With sodium hydride In 1,2-dimethoxyethane at 45℃; for 0.666667h; | 70% |
(R)-2-pentanol
methanesulfonyl chloride
Methanesulfonic acid (R)-1-methyl-butyl ester
Conditions | Yield |
---|---|
With pyridine at 0 - 20℃; | 69% |
With pyridine | 69% |
(R)-2-pentanol
p-trifluoromethylphenyl bromide
Conditions | Yield |
---|---|
Stage #1: (R)-2-pentanol With tris[2-phenylpyridinato-C2,N]iridium(III); nickel(II) bromide dimethoxyethane; 4,4'-Dimethoxy-2,2'-bipyridin; potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.0833333h; Stage #2: p-trifluoromethylphenyl bromide In N,N-dimethyl-formamide at 35℃; for 18h; Sealed tube; Irradiation; | 69% |
(R)-2-pentanol
triphenylene-2,3,6,7,10,11-hexacarboxylic acid hexaethyl ester
Conditions | Yield |
---|---|
With 1-chloro-3-hydroxy-1,1,3,3-tetrabutyldistannoxane In toluene for 216h; Reflux; Inert atmosphere; Dean-Stark; | 65% |
(R)-2-pentanol
[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetic acid
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 24h; Inert atmosphere; | 65% |
(R)-2-pentanol
methyl 4-hydroxy-3-methylbenzoate
Conditions | Yield |
---|---|
Stage #1: methyl 4-hydroxy-3-methylbenzoate With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 0℃; for 0.166667h; Mitsunobu Displacement; Stage #2: (R)-2-pentanol In tetrahydrofuran at 0 - 20℃; for 20h; Mitsunobu Displacement; | 64% |
(1R,2S,5R)-1-(chloromethoxy)-2-isopropyl-5-methylcyclohexane
(R)-2-pentanol
(2R,1'R,2'S,5'R)-2-(2-Isopropyl-5-methylcyclohexyloxymethoxy)pentane
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane 1) 0 deg C, 2 h, 2) r.t., 2 h; | 61% |
With N-ethyl-N,N-diisopropylamine 1) 0 deg C, 2 h, 2) 20 deg C, 2 h; |
(R)-2-pentanol
2-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine
6-amino-2-[(1R)-1-methylbutoxy]-9-(tetrahydro-2H-pyran-2-yl)-9H-purin
Conditions | Yield |
---|---|
Stage #1: (R)-2-pentanol With sodium t-butanolate at 20℃; for 0.333333h; Stage #2: 2-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine at 70℃; for 120h; | 59% |
With sodium t-butanolate at 50℃; for 160h; |
(R)-2-pentanol
(S)-(+)-2-methoxy-2-trifluoromethyl-2-phenylacetyl chloride
Conditions | Yield |
---|---|
With pyridine In dichloromethane | 52% |
(R)-2-pentanol
2,4-dinitrobenzenesulfenyl chloride
Conditions | Yield |
---|---|
With pyridine In 1,2-dichloro-ethane for 0.5h; Ambient temperature; | 41.3% |
(R)-2-pentanol
(R)-methoxytrifluoromethylphenylacetyl chloride
Conditions | Yield |
---|---|
With pyridine In dichloromethane | 41% |
(R)-2-pentanol
(+)(S)-2-chloro-pentane
Conditions | Yield |
---|---|
With phosphorus trichloride |
(R)-2-pentanol
(S)-2-bromopentane
Conditions | Yield |
---|---|
With phosphorus tribromide at 0℃; |
(R)-2-pentanol
(S)-2-iodo-pentane
Conditions | Yield |
---|---|
With carbon disulfide; phosphorous triiodide at 0℃; | |
With hydrogen iodide at 0℃; Erwaermen auf 55grad; |
Conditions | Yield |
---|---|
In n-heptane |
chloro-trimethyl-silane
(R)-2-pentanol
(R)(-)(Pentyl-2-oxy)trimethylsilan
Conditions | Yield |
---|---|
With pyridine; 1,1,1,3,3,3-hexamethyl-disilazane |
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