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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622859Generated: November 1, 2026

Acetic Acid → Cyanocyclohexylideneacetic acid

https://huagongshe.com/reaction/622859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzeneHCID 241—
ReactantCyclohexanoneHCID 7967—
ReactantCyanoacetic acidHCID 9740—
CatalystAmmonium AcetateHCID 517165—
SolventWaterHCID 962—
ProductCyanocyclohexylideneacetic acidHCID 9745790%

Reaction Steps

170 grams (2 moles) of cyanoacetic acid, 196 grams (2 moles) of cyclohexanone, 10 grams (0.13 moles) of ammonium acetate, 24 grams (0.4 moles) of acetic acid, and 380 milliliters of benzene were combined in a 2-liter round-bottomed flask equipped with a reflux condensor and a water separator, and the mixture heated (with reflux) for 6 hours. Upon cooling, the volatile compounds were removed in vacuo, and the residue washed with water to give 360 grams (1.8 moles, 90% yield) of cyclohexylidene cyanoacetic acid. The cyanoacetic acid was distilled under a vacuum of 50 Torricellis (torr.) thereby producing 196 grams (1.6 moles, 81% yield based on cyclohexanone, or 90% yield based on cyclohexylidene cyanoacetic acid) of cyclohexenyl acetic acid nitrile, which had a boiling point of between 115°-120° C. at 50 torr. (As an alternative to distilling the cyanoacetic acid under vacuum in the lastmentioned step, another portion of the cyclohexylidene cyanoacetic acid when heated to 140°-150° C. under a vacuum of 50-70 torr. for 2.5 hours was found to be readily convertible to an impure cyclohexenyl acetic acid nitrile.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04772728
Source datasetuspto-grants-1988_09
ORD IDord-a430b8788cb244ef9e10ca40a04c80cb
Source noteuspto-grants-1988_09