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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342353Generated: October 30, 2026

Water → 4-(2-(4-n-Propylphenyl)ethenyl)cyclohexanone

https://huagongshe.com/reaction/342353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Oxocyclohexane-1-carbaldehydeHCID 11170973—
Reactant4-n-Propylbenzyltriphenyl phosphonium bromideHCID 23118839—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product4-(2-(4-n-Propylphenyl)ethenyl)cyclohexanoneHCID 5391757072.3%

Reaction Steps

Suspension of 114 g of 4-n-propylbenzyltriphenyl phosphonium bromide in 500 ml of THF was stirred under nitrogen gas stream and 32.3 g of potassium-t-butoxide was added thereto at room temperature. After stirred at room temperature for 1 hour, a solution of 31.2 g of 4-formylcyclohexanone in 200 ml of THF was added dropwise to the suspension. After stirred at room temperature for 2 hours, 1 l of water was added thereto and then it was extracted with 1 l of ethyl acetate. Organic layer was washed with water and dried over anhydrous magnesium sulfate, the solvent was distilled off under a reduced pressure, and then 500 ml of heptane was added thereto. Precipitate thus separated was filtered off and purified by a column chromatography over a silica gel by using ethyl acetate/heptane (1/5) as an eluent, and the solvent was distilled off under a reduced pressure to obtain 42 g of 4-(2-(4-n-propylphenyl)ethenyl)cyclohexanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05858275
Source datasetuspto-grants-1999_01
ORD IDord-33b5b69282e94b6a9042cc103cecc836
Source noteuspto-grants-1999_01