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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486054생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/486054

반응식

참여 물질

역할이름HCID투입량
반응물4-ChlorobenzaldehydeHCID 7726—
반응물Sodium HydroxideHCID 14798—
반응물2,2-DimethylcyclopentanoneHCID 138286—
용매EthanolHCID 702—
생성물5-[(4-Chlorophenyl)methylidene]-2,2-dimethylcyclopentan-1-oneHCID 5342102159.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05290791
출처 데이터셋uspto-grants-1994_03
ORD IDord-b1de4ff2d4304c4b8b0fe3c45af4015d
출처 메모uspto-grants-1994_03