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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223718Generated: October 30, 2026

Sodium ethoxide → HCID 20520589, compound

https://huagongshe.com/reaction/223718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
ReactantHCID 12832492HCID 12832492—
Reactant(1R,2R)-2-(Chloromethyl)cyclohexane-1-carbonitrileHCID 12832494—
SolventEthanolHCID 702—
ProductHCID 20520589HCID 2052058978.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium ethylate prepared from sodium (0.23 g) and ethanol (10 ml) was added to ethyl 2-(3-mercaptophenyl)propionate (2.10 g) and the mixture was stirred for a while. Thereto was added trans-2-(chloromethyl)cyclohexanenitrile (1.58 g) and the resulting mixture was refluxed for 5 hours in an oil bath maintained at 100° C. The reaction mixture was evaporated to dryness under reduced pressure and to the residue was added toluene. After removal of the insoluble material by filtration, the solvent was distilled off under reduced pressure. The residue was chromatographed on silica gel, using chloroform as an eluent, to give ethyl 2-[3-(2-cyanocyclohexylmethylthio)phenyl]propionate (2.6 g) as an oil. IRνmaxfilm cm-1 : 2230 (C≡N), 1720 (C=O). MS m/e: 331 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04356186
Source datasetuspto-grants-1982_10
ORD IDord-8ac279c7c02c4b319240ca6387d18c1a
Source noteuspto-grants-1982_10