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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700523Generated: October 27, 2026

Acetone → 2-Chlorobenzylideneacetone

https://huagongshe.com/reaction/1700523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantSodium HydroxideHCID 14798—
Product2-ChlorobenzylideneacetoneHCID 140760—

Reaction Steps

To a mixed solution of acetone (294 ml) and an aqueous solution (1.4 l) of sodium hydroxide (22.0 g) was added 2-chlorobenzaldehyde (70.3 g), and the mixture was stirred at room temperature for 5 hours. Excess acetone was evaporated under reduced pressure, and to the residue was added ethyl acetate (1.4 l). The mixture was subjected to extraction, and the ethyl acetate layer was washed with brine and dried (anhydrous magnesium sulfate). Under reduced pressure, ethyl acetate was evaporated to give crude 2-chlorobenzalacetone (94.6 g) as yellow oil, which was used for the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350749B1
Source datasetuspto-grants-2002_02
ORD IDord-af6a7b13a7db4278bf12b038cc7ee97c
Source noteuspto-grants-2002_02