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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177006Generated: October 31, 2026

1-(3-Chlorophenyl)ethanone → (R)-1-(3-Chlorophenyl)ethanol

https://huagongshe.com/reaction/2177006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Chlorophenyl)ethanoneHCID 14933—
ReactantBorane;tetrahydrofuranHCID 2723981—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product(R)-1-(3-Chlorophenyl)ethanolHCID 695074278%

Reaction Steps

To a solution of borane-tetrahydrofuran (0.647 mL, 0.647 mmol, Aldrich, 1 M solution in THF) and (S)-MeCBS (0.647 mL, 0.647 mmol, Aldrich, 1M solution in toluene) was added simultaneously a solution of 3-chloroacetophenone (1.00 g, 6.47 mmol) in anhydrous tetrahydrofuran (2.42 mL) and a solution of borane-tetrahydrofuran (3.24 mL, 3.24 mmol, Aldrich, 1 M solution in THF) over 30 min at ambient temperature. After complete addition, the reaction mixture was stirred for 10 min, quenched slowly at 0° C. with methanol (0.94 mL) and then saturated HCl in ether (0.12 mL). After stirring at 0° C. for 5 min and ambient temperature for 30 min, the solution was concentrated in vacuo to an oil. The oil was twice diluted with benzene and concentrated in vacuo, diluted with ether, and concentrated in vacuo to an oil. The oil was purified by flash chromatography(silica gel, 20% EA in hexane) to give (R)-1-(3-chlorophenyl)ethanol as a clear colorless oil (0.784 g, 78%). Optical rotation in CHCl3 at 20° C. at concentration 0.220 was +40.9° (Literature, Bull. Chem. Soc. Jpn. 1996, 69(4), 1079-1085, optical rotation in CHCl3 at 21° C. at concentration 0.220 was +44°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067897B2
Source datasetuspto-grants-2015_06
ORD IDord-cd0c8f07bb3e4858818e7dd63a01ae17
Source noteuspto-grants-2015_06