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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449320Generated: October 31, 2026

Isoprene → 1-(4,6,6-Trimethylcyclohex-3-en-1-yl)ethan-1-one

https://huagongshe.com/reaction/1449320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopreneHCID 6557—
ReactantMesityl oxideHCID 8858—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventBenzeneHCID 241—
Product1-(4,6,6-Trimethylcyclohex-3-en-1-yl)ethan-1-oneHCID 2054723976.3%

Reaction Steps

A flask is charged with 63 g of aluminium chloride and 2160 ml of anhydrous benzene. The apparatus is filled with nitrogen and 441 g of mesityl oxide are added, whilst stirring and maintaining the temperature of the mixture at +15°. The mixture is then left for 30 minutes at this temperature, whilst stirring. 1224 g of isoprene dissolved in 1800 ml of anhydrous benzene are then added in the course of 1 hour at +15°. Reaction is then effected for 20 hours at 16° followed by 6 hours at +25°, with stirring. The contents of the flask are then transferred to a separating funnel and the product is washed twice with 500 ml of 10% hydrochloric acid, once with 500 ml of water, once with 500 ml of a 9% solution of sodium bicarbonate and twice with 500 ml of water. The benzene is distilled off on a water bath, finally, under a pressure of 30 mm of mercury. 1070 g of crude product are obtained, which are purified in a Vigreux flask under a pressure of 1 mm of mercury. 560 g of 1,5,5-trimethyl-4-acetyl-cyclohex-1-ene (76.3%) are obtained, having the following physical properties:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04190561
Source datasetuspto-grants-1980_02
ORD IDord-f373357e1a0748dfb4887682897ae4e8
Source noteuspto-grants-1980_02