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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576203Generated: November 3, 2026

Acetic Acid → Cyclohexanecarbonitrile, 1-(1-naphthalenyl)-4-oxo-

https://huagongshe.com/reaction/1576203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSulfuric AcidHCID 1118—
ReactantHCID 12230237HCID 12230237—
SolventWaterHCID 962—
ProductCyclohexanecarbonitrile, 1-(1-naphthalenyl)-4-oxo-HCID 1223024076%

Reaction Steps

A mixture of 16.73 g. (0.055 mole) of methyl 5-cyano-5-(1-naphthyl)-2-oxocyclohexanecarboxylate (prepared in Example 11) in 400 ml. of acetic acid and 200 ml. of 10% sulfuric acid is stirred mechanically for about 44 hours. The mixture is then allowed to cool and diluted with water. This mixture is extracted thoroughly with benzene. The organic layer is successively washed with water, sodium bicarbonate solution and brine and evaporated to dryness. The solid residue is recrystallized from acetone to give 10.3 g. (76% yield) of 4-cyano-4-(1-naphthyl)cyclohexanone, having a melting point of 213° to 215°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03979444
Source datasetuspto-grants-1976_09
ORD IDord-0c2df48257f54f2ca34ef7dc2613c2a0
Source noteuspto-grants-1976_09