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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236876Generated: October 30, 2026

Hydrogen Bromide → alpha-Hydroxyacetophenone

https://huagongshe.com/reaction/236876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantMethanolHCID 887—
ReactantAcetophenoneHCID 7410—
ReactantBromineHCID 24408—
SolventWaterHCID 962—
Productalpha-HydroxyacetophenoneHCID 68490—

Reaction Conditions

Temperature60 °C

Reaction Steps

About 13 parts of bromine was added with stirring to a mixture of 474.6 parts of acetophenone in about 640 parts of methanol, while the mixture was stirred and maintained at a temperature between 5°-10° C. Hydrogen bromide gas was then introduced into the mixture until bromine coloration disappeared, at which point an additional amount of bromine was added over a 2 hour period to make a total of 631.3 parts. There was then added 71 parts of water while the mixture was stirred and externally cooled for a period of about 30 minutes. An excess of about 2700 parts of water was then slowly added to effect the precipitation in the form of crystals of α-bromo acetophenone from the mixture. The crystals were decanted by means of a vacuum siphon, washed, then neutralized with a 20% sodium hydroxide solution and decanted to dryness. There was then added about 940 parts water, 1600 parts of methanol, 333 parts of sodium bicarbonate and a sodium formate solution prepared from 161 parts of 90% formic acid and sufficient sodium hydroxide to neutralize the acid. The mixture was heated at 60° C. with vigorous stirring for 7 hours after which time it was cooled to ambient temperature and filtered. Based on method of preparation and gas chromatographic analysis of the mixture there was produced α-hydroxy acetophenone in quantitative yields.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04158094
Source datasetuspto-grants-1979_06
ORD IDord-b175cd0cc88d4435bf78265a833dfcc8
Source noteuspto-grants-1979_06