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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450677Generated: October 31, 2026

Cyclohexanone Oxime → 3-[(Cyclohexylideneamino)oxy]propanoic acid

https://huagongshe.com/reaction/1450677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanone OximeHCID 7517—
ReactantEthyl AcrylateHCID 8821—
ReactantPotassium HydroxideHCID 14797—
SolventEthanolHCID 702—
Product3-[(Cyclohexylideneamino)oxy]propanoic acidHCID 1997720924,503%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 32.8 g (0.29 mol) of cyclohexanone oxime, 26 g (0.26 mmol) of ethyl acrylate, 26 ml (0.052 mol) of a 2N solution of KOH in ethanol and 150 ml of ethanol is stirred for 96 hours at 60° C. and afterwards concentrated on a vacuum rotary evaporator. The residue (an orange oil) is dissolved in 175 g (0.31 tool) of a 10% solution of KOH in ethanol and the solution is heated for 1 hour to 60° C. The solvent is distilled off and the solid residue is taken up in water. After acidification with c. 15 ml of conc. hydrochloric acid and extraction with ethyl acetate, the organic phase is washed with water, dried over Na2SO4 and concentrated on a vacuum rotary evaporator. Distillation of the residue yields 11.8 g (25%) of the desired acid as an orange liquid. The boiling point is 135° C./0.05 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602196
Source datasetuspto-grants-1997_02
ORD IDord-2f76d6ee00514261b05b6fa40148cab8
Source noteuspto-grants-1997_02