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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416168Generated: November 3, 2026

Ethanone, 1-(2,6,6-trimethyl-3-cyclohexen-1-yl)- → Trans-4-Acetyl-3,5,5-Trimethylcyclohexene

https://huagongshe.com/reaction/2416168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanone, 1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-HCID 117287—
CatalystRhodium chloride trihydrateHCID 11459718—
SolventEthanolHCID 702—
ProductTrans-4-Acetyl-3,5,5-TrimethylcyclohexeneHCID 54437493—

Reaction Steps

In a 200-ml four-necked flask equipped with a thermometer, condenser and a stirrer, placed were 2,6,6-trimethyl-3-cyclohexenyl methyl ketone (10 g) synthesized in Referential Example 1, ethyl alcohol (40 ml) and rhodium trichloride trihydrate (0.9 g). Under stirring, they were reacted at 90° C. for 24 hours. The reaction mixture at this time was sampled and analyzed by gas chromatography, resulting in that the content of trans-2,6,6-trimethyl-3-cyclohexenyl methyl ketone was 11%, while those of 2,6,6-trimethyl-2-cyclohexenyl methyl ketone and 2,6,6-trimethyl-1-cyclohexenyl methyl ketone produced by the above reaction were 87% and 2%, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822121B2
Source datasetuspto-grants-2004_11
ORD IDord-0e4410c17a534a3fab617a724f481df4
Source noteuspto-grants-2004_11