Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605662Generated: October 26, 2026

Carbon Dioxide → (E)-4-(3-Chloro-4-cyclohexyl-phenyl)-3-pentene-2-one

https://huagongshe.com/reaction/1605662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl (2E)-3-ethoxy-2-butenoateHCID 5354173—
Reactant1-(3-Chloro-4-cyclohexylphenyl)ethanoneHCID 10900646—
SolventDimethylformamideHCID 6228—
Product(E)-4-(3-Chloro-4-cyclohexyl-phenyl)-3-pentene-2-oneHCID 68133285—

Reaction Steps

87.6 Gm (0.781 mol) of potassium-tert.butylate were added all at once to a solution of 185.0 gm (0.781 mol) of 3'-chloro-4'-cyclohexyl-acetophenone and 123.0 gm (0.777 mol) of ethyl (E)-3-ethoxy-crotonate in 1.1 liters of anhydrous dimethyl formamide, whereby the temperature rose spontaneously from +20° to +38°C and the mixture turned deep red. The mixture was stirred for another hour with the temperature being maintained at 32°-35°C, and then 200 ml of concentrated hydrochloric acid added dropwise to the still warm mixture, and the resulting mixture was heated for 60 minutes at a temperature of 90°-100°C. After carbon dioxide evolution had ceased, the cooled mixture was stirred into 1 liter of ice water, and the aqueous mixture was exhaustively extracted with ether. The combined ether extracts were washed with water, dried over sodium sulfate and concentrated by evaporation. The residue was distilled in a vacuum (b.p. 175°-183°C at 0.1 mm Hg) and subsequently recrystallized twice from methanol, in the presence of activated charcoal. The colorless crystals, m.p. 56.5°-57.5°C were obtained with a yield of 132 gm (61% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950427
Source datasetuspto-grants-1976_04
ORD IDord-2b6409e3604a463ca5de409ad9f40d10
Source noteuspto-grants-1976_04