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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021349Generated: October 29, 2026

Sodium borohydride → (2-Bromo-4-chlorophenyl)methanol

https://huagongshe.com/reaction/1021349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Bromo-4-chlorobenzaldehydeHCID 13154710—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(2-Bromo-4-chlorophenyl)methanolHCID 5404976480.4%

Reaction Steps

A solution of 2-bromo-4-chlorobenzaldehyde (21.95 g; 100.0 mmol) in 200 mL methanol was stirred and cooled in an ice bath for 15 minutes, and solid sodium borohydride (1.9 g; 50.0 mmol) was added. A yellow color formed and there was copious gas evolution. Stirring was continued in the bath for 1 hour. The solution was diluted with 200 mL water, and then the methanol was evaporated on a rotary evaporator. The residual mixture was extracted with 200 mL EtOAc. The organic layer was washed with 50 mL brine, then dried over sodium sulfate and evaporated. The residual solid was washed out of the flask with hexane and collected by filtration, ground with a mortar and pestle to break up the chunks, then washed with hexane and air-dried on the filter to give 17.8 g of (2-bromo-4-chlorophenyl)methanol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716498B2
Source datasetuspto-grants-2014_05
ORD IDord-da0fda51d24e49b180299ac4ffa81015
Source noteuspto-grants-2014_05