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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912293Generated: October 30, 2026

Sodium borohydride → 1-(5-Bromo-2-chlorophenyl)ethanol

https://huagongshe.com/reaction/1912293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(5-Bromo-2-chlorophenyl)ethan-1-oneHCID 13628145—
SolventMethanolHCID 887—
Product1-(5-Bromo-2-chlorophenyl)ethanolHCID 5876264499.3%

Reaction Steps

Sodium borohydride (1.182 g, 51.4 mmol) was added to a stirred solution of 1-(5-bromo-2-chlorophenyl)ethanone (10 g, 42.8 mmol) in methanol at 0° C., The resulting bubbling white mixture was allowed to warm to room temperature and stirred for 2 h. The reaction mixture was quenched with acetone (50 mL) and concentrated by rotary evaporation. The residue was partitioned between ethyl acetate and water. The organic phase was dried and concentrated to yield the title compound (10 g, 42.5 mmol, 99% yield) as a white solid: 1H NMR (CDCl3): δ 7.75 (d, 1H), 7.32 (m, 1H), 7.19 (m, 1H), 5.23 (q, 1H), 1.95 (d, 1H), 1.48 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609592B2
Source datasetuspto-grants-2013_12
ORD IDord-8feae0ab500d4dbfb65229e4b782c8a7
Source noteuspto-grants-2013_12