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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237132Generated: October 25, 2026

Allyl bromide → 2-Allyl-cyclohexane-1,3-dione

https://huagongshe.com/reaction/237132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1,2-CyclohexanedioneHCID 13006—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium HydroxideHCID 14798—
SolventEthyl AcetateHCID 8857—
Product2-Allyl-cyclohexane-1,3-dioneHCID 566005—

Reaction Steps

Allyl bromide (195 g., 1.62 mol.) was added over a 15 minute period to a stirred ice-cold mixture of cyclohexanedione (165 g., 1.47 mol.), copper-bronze (4.5 g.), and 330 ml. of 20% by weight aqueous potassium hydroxide. After 6 hours, the reaction was mixed with 1500 ml. of a 5% by weight aqueous sodium hydroxide solution and 1000 ml. of ethyl ether, filtered and the separated water layer acidified with 4N aqueous hydrochloric acid to pH 1. A brown solid (188 g.) formed upon refrigeration at 0° C. The solid was taken up in ethyl acetate and the solution was washed with water (3×150 ml.), dried (MgSO4), treated with charcoal, and condensed until turbid. Upon cooling, 126 g. (57%) of 2-allyl-1,3-cyclohexanedione was collected, m.p. 125°-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04159386
Source datasetuspto-grants-1979_06
ORD IDord-dad3354ab2574929a343c8536aa9769c
Source noteuspto-grants-1979_06