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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567129Generated: October 29, 2026

Acetone → 1-[3-(Trifluoromethyl)phenyl]but-1-en-3-one

https://huagongshe.com/reaction/567129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Reactant3-(Trifluoromethyl)benzaldehydeHCID 67990—
Product1-[3-(Trifluoromethyl)phenyl]but-1-en-3-oneHCID 14493488.7%

Reaction Steps

In a 250 ml single neck flask was charged 7.5 g (43.1 mmoles,1.0 eq) of m-trifluoromethylbenzaldehyde dissolved in 15 ml of acetone. To this was added 17.2 g of 10% aqueous sodium hydroxide solution (43 mmoles, 1.0 eq), dropwise and during the course of addition, temperature was kept no higher than 25° C., while the mixture was agitated continuously for 30 minutes. To the mixture was added 50 ml of water, followed by 100 ml of ethyl acetate, the phases were separated and the organic phase was washed with water three times and then dried, and concentrated to obtain 9.5 g of 4-(3-trifluoromethylphenyl)-3-buten-2-one as a faintly yellow oil in 88.7% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177462B1
Source datasetuspto-grants-2001_01
ORD IDord-8d997b04a129467db86cf4a8b5980307
Source noteuspto-grants-2001_01