Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905143Generated: October 25, 2026

Potassium Hydroxide → 3-(2-Ethylhexanoyloxy)-5,5-dimethyl-2-(2',5'-dimethylphenyl)-2-cyclohexenone

https://huagongshe.com/reaction/905143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2-Ethylhexanoyl chlorideHCID 79103—
Reactant2-(2',5'-Dimethylphenyl)-5,5-dimethyl-1,3-cyclohexanedioneHCID 12876602—
CatalystDicyclohexano-18-crown-6HCID 85955—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
Product3-(2-Ethylhexanoyloxy)-5,5-dimethyl-2-(2',5'-dimethylphenyl)-2-cyclohexenoneHCID 2020651092.3%

Reaction Steps

A suspension of 1.50 g (6.14 mmol) of 2-(2',5'-dimethylphenyl)-5,5-dimethyl-1,3-cyclohexanedione in 15 ml of dry benzene was prepared and 0.49 g (7.37 mmol) of 85% powdered potassium hydroxide was added, followed by 1 drop of dicyclohexyl-18-crown-6-ether. After stirring for 30 minutes, 1.20 g (7.37 mmol) of 2-ethylhexanoyl chloride was added, and the reaction mixture refluxed for 12 hrs. The reaction mixture was cooled to room temperature, taken up in 150 ml ether and 50 ml of water, washed three times with 0.25 N, NaOH, two times with water, two times with 6 N HCl, and once more with water. The ether solution was dried and stripped to leave 2.10 g (92% yield) of 3-(2-ethylhexanoyloxy)-5,5-dimethyl-2-(2',5'-dimethylphenyl)-2-cyclohexenone as a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04422870
Source datasetuspto-grants-1983_12
ORD IDord-d9aa4d897b7a423a83ed962dfc0becdd
Source noteuspto-grants-1983_12