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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927294Generated: October 31, 2026

Diethanolamine → (1R)-1-(2-bromo-3-methylphenyl)ethanol

https://huagongshe.com/reaction/1927294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethanolamineHCID 8113—
ReactantChlorobis((1S,2R,3S,5S)-2,6,6-trimethylbicyclo(3.1.1)hept-3-yl)boraneHCID 9923113—
ReactantHCID 57514834HCID 57514834—
SolventTetrahydrofuranHCID 8028—
Product(1R)-1-(2-bromo-3-methylphenyl)ethanolHCID 5857244999%

Reaction Conditions

Temperature-20 °C

Reaction Steps

(+)-B-chlorodiisopinocampheylborane (8.46 g, 26.4 mmol) was dissolved in tetrahydrofuran (150 mL), cooled to −20° C., slowly added dropwise with a solution of 1-(2-bromo-3-methylphenyl)ethanone (4.30 g, 20.3 mmol) described in US 2007/167506 in tetrahydrofuran (50 mL), and stirred for 18 hours. The reaction solution was added with diethanolamine (6.38 g, 60.8 mmol), cooled to room temperature, and stirred at room temperature for 3 hours. The reaction solution was concentrated under reduced pressure and added with n-hexane (100 mL). The precipitated solids were filtered off and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=4/1) to give the title compound as a white solid (4.30 g, yield 99%, 95.6% ee).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183272B2
Source datasetuspto-grants-2012_05
ORD IDord-2deb15fdc08444289e13499f57b05116
Source noteuspto-grants-2012_05