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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576200Generated: November 2, 2026

Acetic Acid → 1-(4-Chlorophenyl)-4-oxocyclohexanecarbonitrile

https://huagongshe.com/reaction/1576200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSulfuric AcidHCID 1118—
Reactant2-Carbomethoxy-4-(p-chlorophenyl)-4-cyanocyclohexanoneHCID 12230234—
SolventWaterHCID 962—
Product1-(4-Chlorophenyl)-4-oxocyclohexanecarbonitrileHCID 1223023882%

Reaction Steps

A mixture of 29.8 g. (0.102 mole) of methyl 5-cyano-5-(4-chlorophenyl)-2-oxocyclohexanecarboxylate (prepared in Example 7) in 660 ml. of acetic acid and 330 ml. of 10% sulfuric acid is stirred mechanically on a steam bath for about 24 hours. The mixture is then allowed to cool and diluted with water. This mixture is extracted thoroughly with benzene. The organic layer is washed successively with water, sodium bicarbonate solution and brine and evaporated to dryness. The solid residue is recrystallized from ether to give 19.49 g. (82% yield) of 4-cyano-4-(4-chlorophenyl)cyclohexanone, having a melting point of 94.5° to 97°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03979444
Source datasetuspto-grants-1976_09
ORD IDord-0f1876c50e4744a7893575c4349be497
Source noteuspto-grants-1976_09