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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304399Generated: November 1, 2026

Bromomethyl 4-methoxyphenyl ketone → 2-Bromo-1-(4-methoxyphenyl)ethan-1-ol

https://huagongshe.com/reaction/2304399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product2-Bromo-1-(4-methoxyphenyl)ethan-1-olHCID 14288506109.4%

Reaction Steps

0.826 g (21.8 mmol) of sodium borohydride was added to 2-bromo-4′-methoxy-acetophenone (10 g, 43.7 mmol) in methanol (200 ml) and the mixture was stirred for 1 hour at room temperature. The mixture was concentrated in vacuo and saturated aqueous sodium chloride was added to the residue and the product was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and concentrated in vacuo to give 2-bromo-1-(4′-methoxyphenyl) ethanol (11.05g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06436922B1
Source datasetuspto-grants-2002_08
ORD IDord-cb65006880f048a69305844550d0db78
Source noteuspto-grants-2002_08