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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679669Generated: October 30, 2026

Methanol → 2-Bromo-1-(1-methylcyclohexyl)ethan-1-one

https://huagongshe.com/reaction/1679669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantChloroformHCID 6212—
ReactantBromineHCID 24408—
Reactant1-(1-methylcyclohexyl)ethanoneHCID 544198—
CatalystBromineHCID 24408—
SolventWaterHCID 962—
Product2-Bromo-1-(1-methylcyclohexyl)ethan-1-oneHCID 21475011—

Reaction Steps

A solution of 328 g. bromine in 300 ml. chloroform was added gradually to a stirred solution of 300 g. 1-methylcyclohexyl methyl ketone in 100 ml. methanol. After the addition of a few drops of bromine solution at 15° C. the reaction mixture was cooled and maintained between 0° - 5° C. The reaction mixture was stirred for 10 minutes, after the addition of bromine had been completed, and then poured on to a mixture of crushed ice and water. The water layer was separated from the organic liquid and extracted with methylene chloride. The extract and the organic portion were combined and washed with water followed by a saturated solution of sodium bicarbonate and then finally with water. After drying over calcium chloride the liquid was evaporated and distilled to give bromomethyl 1-methylcyclohexyl ketone, b.p. 76° - 78° C./0.1 mm. Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04081540
Source datasetuspto-grants-1978_03
ORD IDord-3a23297d93a3499aad04d3d9c5ab1bfb
Source noteuspto-grants-1978_03