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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834320Generated: October 26, 2026

Acetonitrile → 3-Acetoxycyclohexene

https://huagongshe.com/reaction/1834320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantCyclohexeneHCID 8079—
Reactanttert-Butyl peroxybenzoateHCID 11966—
Reactant(S)-(-)-N-salicylidene-1-phenyl-2-(p-tolyl)ethylamineHCID 136388393—
CatalystCopperHCID 23978—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
Product3-AcetoxycyclohexeneHCID 11116148—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 0.50 g of the copper complex of (S)-(-)-N-salicylidene-1-phenyl-2-(p-tolyl)ethylamine, 0.045 g of copper powder, 25 ml of cyclohexene, 25 ml of acetonitrile, 5 ml of acetic acid and 5 ml of t-butyl peroxybenzoate was heated with stirring at 70° C for 7 hours in a nitrogen atmosphere. After cooling, the reaction mixture was admixed with 50 ml of benzene, washed successively with a 2N aqueous hydrochloric acid solution, water, an aqueous solution saturated with sodium hydrogen carbonate and an aqueous solution saturated with sodium chloride, and dried over anhydrous sodium sulfate. After evaporating the solvent, the residue was distilled under reduced pressure to obtain 1.88 g of 2-cyclohexenyl acetate. B.P. 75°-76° C/21 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04069385
Source datasetuspto-grants-1978_01
ORD IDord-62185435f3b64c9495415c3306017607
Source noteuspto-grants-1978_01