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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567125Generated: November 1, 2026

Acetone → (E)-4-(2-Chloro-phenyl)-but-3-en-2-one

https://huagongshe.com/reaction/567125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Product(E)-4-(2-Chloro-phenyl)-but-3-en-2-oneHCID 537282076.9%

Reaction Steps

In a 250 ml single neck flask was charged 14 g (99.6 mmoles, 1.0 eq) of o-chlorobenzaldehyde dissolved in 30 ml of acetone. To this was added 5 g of a 10% aqueous sodium hydroxide solution (12.5 mmoles, 0.125 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 13.8 g of (E)-4-(2-chlorophenyl)-3-buten-2-one as a faintly yellow oil in 76.9% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177462B1
Source datasetuspto-grants-2001_01
ORD IDord-59b5c8332ea744a580b2ce941167b7fe
Source noteuspto-grants-2001_01