Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501014Generated: October 31, 2026

Methanol → (R)-1-(4-Bromophenyl)ethanol

https://huagongshe.com/reaction/1501014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactantp-BromoacetophenoneHCID 7466—
Reactant(3aS)-1-methyl-3,3-diphenyl-hexahydropyrrolo(1,2-c)(1,3,2)oxazaboroleHCID 2734713—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(R)-1-(4-Bromophenyl)ethanolHCID 695017392%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution of 4-bromoacetophenone (5.0 g, 25 mmol) and (S)-2-Methyl-CBS-oxazaborolidine (1.25 mL, 1 M) in anhydrous dichloromethane (80 mL) was added borane-methyl sulfide complex (2.1 g, 27 mmol) over 1 hour at −20° C. After addition completed, the mixture was stirred at −20° C. for 2 hours, then stirred at room temperature for 12 hours. After the reaction, methanol (20 mL) was added, and stirred for 0.5 hour. Then the mixture was diluted with water (100 mL) and the organic phase was dried over anhydrous sodium sulfate. The mixture was filtered and the filtrate was concentrated. The residue was purified by column chromatography (silica gel, ethyl acetate/petroleum ether=1:8) to give pure product (R)-1-(4-bromophenyl)ethanol as a white solid (4.6 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206128B2
Source datasetuspto-grants-2015_12
ORD IDord-18c5057a1ad64e08b9f1d921a11a57aa
Source noteuspto-grants-2015_12