Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029935Generated: October 30, 2026

Methyl vinyl ketone → 4,4-Bis(3-fluorophenyl)cyclohexenone

https://huagongshe.com/reaction/1029935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl vinyl ketoneHCID 6570—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 54068354HCID 54068354—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product4,4-Bis(3-fluorophenyl)cyclohexenoneHCID 54307328—

Reaction Conditions

Temperature0 °C

Reaction Steps

Butenone (50.4 cc) is added to a solution of bis-(3-fluorophenyl)acetaldehyde (144.5 g) in ethyl ether (500 cc) and then, after cooling to 0° C., a solution of potassium hydroxide (13.9 g) in ethanol (89 cc) is added dropwise. The reaction mixture is stirred for 2 h at 0° C. and then for 16 hours at 25° C. and diluted with ethyl acetate (300 cc) and water (500 cc). The aqueous phase is washed with ethyl acetate (300 cc). The combined organic phases are washed with saturated sodium chloride solution (500 cc), dried over magnesium sulphate and concentrated under reduced pressure (2.7 kPa). The residue is chromatographed (in two passes) on silica gel (particle size 0.04-0.063 mm, columns 8.5 cm in diameter and 34 cm high), eluting under a nitrogen pressure of 0.5 bar with a mixture of cyclohexane and ethyl acetate (90/10). 4,4-bis-(3-Fluorophenyl)-cyclohexenone (90.3 g) is obtained in the form of white crystals. m.p.=95° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102667
Source datasetuspto-grants-1992_04
ORD IDord-c72e6252e77d42bda61bdea4f6c0e687
Source noteuspto-grants-1992_04