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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796836Generated: November 3, 2026

Acetic Acid → CYANO-CYCLOHEXYLIDENE-ACETIC ACID METHYL ESTER

https://huagongshe.com/reaction/1796836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl cyanoacetateHCID 7747—
ReactantCyclohexanoneHCID 7967—
ReactantAmmonium AcetateHCID 517165—
SolventBenzeneHCID 241—
ProductCYANO-CYCLOHEXYLIDENE-ACETIC ACID METHYL ESTERHCID 11229121—

Reaction Steps

To a solution of cyclohexanone (84.1 g, 1 mol) in dry benzene (100 mL) was added methyl cyanoacetate (99.1 g, 1 mol), ammonium acetate (10 g) and glacial acetic acid (20 mL). The reaction mixture was heated to reflux using Dean-Stark apparatus for 12 hours and allowed to cool to room temperature. Excess of solvents was removed in vacuo and the residue was dissolved in EtOAc (400 mL). The organic layer was washed with water, dried over sodium sulfate and evaporated to give cyano-cyclohexylidene-acetic acid methyl ester as pale yellow oil. Further purification of the pale yellow oil by distillation (10 mm Hg, 150–155° C.) gave product the title compound (110 g, 61%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 1.70–1.85 (m, 6H), 2.70 (t, 2H), 3.00 (t, 2H), 3.80 (s, 3H); 13C NMR (75 MHz, CDCl3) δ 25.9, 28.6, 28.9, 31.9, 37.2, 52.8, 101.9, 115.8, 162.7, 180.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030267B2
Source datasetuspto-grants-2006_04
ORD IDord-27b12dff384448308f0345c7a31f015d
Source noteuspto-grants-2006_04