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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779978Generated: November 2, 2026

4-Chlorobenzaldehyde → 5-[(4-Chlorophenyl)methylidene]-2,2-dimethylcyclopentan-1-one

https://huagongshe.com/reaction/1779978

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSodium HydroxideHCID 14798—
Reactant2,2-DimethylcyclopentanoneHCID 138286—
SolventEthanolHCID 702—
Product5-[(4-Chlorophenyl)methylidene]-2,2-dimethylcyclopentan-1-oneHCID 5342102159.7%

Reaction Steps

10% aqueous sodium hydroxide solution (100 ml) is added to a mixture of 2,2-dimethylcyclopentanone (10 g) and 4-chlorobenzaldehyde (13.8 g) in ethanol (100 ml) at 0° C. After 30 minutes, a thick slurry is filtered and the solid is washed and then dried. 2,2-Dimethyl-5-(4-chlorobenzylidene)-1-cyclopentanone (12.5 g), m.p. 120° C., is obtained. This compound, dissolved in THF (50 ml), is added to a solution formed in the following manner: sodium hydride (80% dispersion in mineral oil) (1.9 g) in anhydrous DMSO (50 ml) is heated to 80° C. until the solid has dissolved completely. The solution is then diluted with THF (100 ml) and then cooled to -10° C. A solution of trimethylsulphonium iodide (11.5 g) in dimethyl sulphoxide (80 ml) is added to the mixture in the course of 10 minutes and the mixture is stirred for 15 minutes at -10° C. A solution of 2,2-dimethyl-4-chloro-5-(4-chlorobenzylidene)-1-cyclopentanone (11.8 g) in THF (100 ml) is then added.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629330
Source datasetuspto-grants-1997_05
ORD IDord-ec66fc403c1b460f8af136602555dffa
Source noteuspto-grants-1997_05