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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974214Generated: November 3, 2026

Benzene → 2-Cyclohexen-1-one, 2,6,6-trimethyl-3-(2-methylpropoxy)-

https://huagongshe.com/reaction/1974214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantIsobutanolHCID 6560—
ReactantHCID 70585111HCID 70585111—
SolventWaterHCID 962—
Product2-Cyclohexen-1-one, 2,6,6-trimethyl-3-(2-methylpropoxy)-HCID 10921765—

Reaction Steps

The compound 2,6,6-trimethylcyclohexen-1,3-dione (43.6 g) was added to a mixture of benzene (250 ml), isobutanol (50 ml) and PTSA (500 mg) and heated under reflux for 3 hr in conjunction with a Dean and Stark water separator. The reaction was then cooled to room temperature, washed with aqueous sodium carbonate solution and brine and taken to dryness "in vacuo". Distillation of residue through a 6 inch vacuum jacketed vigreaux column yielded pure 2,6,6-trimethyl-3-isobutoxycyclohex-2-en-1 one (54.6 g) bp 104°-107°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04000198
Source datasetuspto-grants-1976_12
ORD IDord-7e5a5b28ea4845dda657d116fed47b92
Source noteuspto-grants-1976_12