Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973265Generated: October 29, 2026

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

https://huagongshe.com/reaction/1973265

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 numberUS03996366
Source datasetuspto-grants-1976_12
ORD IDord-88ffa17e74564b98bbcc7c29b17f931d
Source noteuspto-grants-1976_12