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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65808Generated: October 25, 2026

4-(Acetyloxy)-2-butanone → 2,3,6-Trimethylcyclohex-2-en-1-one

https://huagongshe.com/reaction/65808

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Acetyloxy)-2-butanoneHCID 139100—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product2,3,6-Trimethylcyclohex-2-en-1-oneHCID 3016843—

Reaction Steps

130 g of 1-acetoxybutan-3-one and sodium methylate solution in methanol are dripped in the course of one hour from separate supply vessels while stirring into 400 g of boiling diethyl ketone at such a rate that the reaction mixture remains constantly alkaline. A total of 190 g of a 30% by weight sodium methylate solution is used up in this way. The whole is then heated under reflux for another hour and then neutralized with glacial acetic acid. Deposited sodium acetate is filtered off and the filtrate is subjected to fractional distillation. 81 g of 2,3,6-trimethyl-2-cyclohexen-1-one is obtained as well as traces of 4-methyl-3-ethyl-2-cyclohexen-1-one. The yield with reference to 1-acetoxybutan-3-one is 59%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04128728
Source datasetuspto-grants-1978_12
ORD IDord-6378b9e4c99d40c6811d8c8750d9496a
Source noteuspto-grants-1978_12