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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65805Generated: October 25, 2026

Hydroquinone → 2,3,6-Trimethylcyclohex-2-en-1-one

https://huagongshe.com/reaction/65805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantMethyl vinyl ketoneHCID 6570—
ReactantAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
SolventEthyl ketoneHCID 7288—
Product2,3,6-Trimethylcyclohex-2-en-1-oneHCID 3016843—
Product4-Methyl-3-ethyl-2-cyclohexen-1-oneHCID 12540304—

Reaction Steps

A mixture of 70 g of methyl vinyl ketone, 10 g of water and 0.1 g of hydroquinone is dripped in the course of one hour into a mixture of 400 g of diethyl ketone and 10 g of a 30% by weight methanolic solution of sodium methylate which is boiling under reflux. The whole is then heated for another two hours under reflux. The mixture obtained is neutralized with glacial acetic and then filtered. Excess diethyl ketone and the water present are distilled off and the residue is fractionated in vacuo. 81 g of 2,3,6-trimethyl-2-cyclohexen-1-one having a boiling point of 89° C. at 12 mm Hg and 9 g of 4-methyl-3-ethyl-2-cyclohexen-1-one having a boiling point of 102° C. at 12 mm Hg are obtained. The total yield of cyclohexenone is 65% with reference to methyl vinyl ketone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04128728
Source datasetuspto-grants-1978_12
ORD IDord-b41c8aabc0ed4695882d0191604779f4
Source noteuspto-grants-1978_12