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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769582Generated: November 2, 2026

Water → Ethyl cyclohexylideneacetate

https://huagongshe.com/reaction/1769582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-(3,4,5-Trifluorophenyl)cyclohexan-1-oneHCID 21993284—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductEthyl cyclohexylideneacetateHCID 73776—

Reaction Steps

A suspension of triethyl phosphonoacetate (21.8 g) in THF (50 ml) was stirred in a nitrogen gas stream, followed by adding potassium-t-butoxide (11.8 g) little by little at room temperature, stirring the reaction solution at room temperature for one hour, dropwise adding a solution of 4-(3',4',5'-trifluorophenyl)cyclohexanone (20 g) in THF (50 ml), stirring at room temperature for 2 hours, adding to water (100 ml), extracting with ethyl acetate (100 ml), washing the organic layer with water, drying over anhydrous MgSO4 and concentrating the solvent under reduced pressure, to obtain 4-(3',4',5'-trifluorophenyl))ethoxycarbonylmethylenecyclohexane (18.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05382379
Source datasetuspto-grants-1995_01
ORD IDord-06f97a4fe8a04746bd885910931cd362
Source noteuspto-grants-1995_01