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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602068Generated: November 2, 2026

Benzonitrile → Cyclohexanone

https://huagongshe.com/reaction/1602068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
ReactantN-HydroxyphthalimideHCID 10665—
SolventCyclohexaneHCID 8078—
ProductCyclohexanolHCID 79661%
ProductCyclohexanoneHCID 796710%

Reaction Steps

To 20 ml of benzonitrile were added 10 mmol of cyclohexane, 1 mmol of N-hydroxyphthalimide, 0.01 mmol of cobalt acetate Co(OAc)2, and 0.05 mmol of acetylacetonatocobalt Co(AA)2 and the resultant mixture was stirred under an oxygen atmosphere at a temperature of 75° C. for 16 hours. The products in the reaction mixture were analyzed by gas chromatography, and, as a result, cyclohexane was converted into cyclohexanone (yield 10%) and cyclohexanol (yield 1%) with a conversion of 12%. Adipic acid was not detected. The selectivity of K/A oil was 93% based on the consumed cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981420
Source datasetuspto-grants-1999_11
ORD IDord-65977e8ac92d4e15b1f64bae111a8cc9
Source noteuspto-grants-1999_11