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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 486054Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/486054

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-ChlorobenzaldehydeHCID 7726—
EduktSodium HydroxideHCID 14798—
Edukt2,2-DimethylcyclopentanoneHCID 138286—
LösungsmittelEthanolHCID 702—
Produkt5-[(4-Chlorophenyl)methylidene]-2,2-dimethylcyclopentan-1-oneHCID 5342102159,7%

Reaktionsschritte

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 (s0% 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05290791
Quelldatensatzuspto-grants-1994_03
ORD IDord-b1de4ff2d4304c4b8b0fe3c45af4015d
Quellennotizuspto-grants-1994_03