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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1504생성일: 2026년 10월 23일

Dimethylformamide → 2-(4-Chlorophenyl)-3-(dimethylamino)acrylaldehyde

https://huagongshe.com/ko/reaction/1504

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물(4-Chlorophenyl)acetic acidHCID 15880—
반응물Phosphorus oxychlorideHCID 24813—
용매TolueneHCID 1140—
생성물2-(4-Chlorophenyl)-3-(dimethylamino)acrylaldehydeHCID 3448972—

반응 단계

Phosphorus oxychloride (92 g) was added dropwise to stirred DMF (78 ml) between 10°-15° C. To the resulting slurry was added 4-chlorophenylacetic acid (34.12 g). The resulting mixture was stirred at room temperature for one half hour and then heated to 70°-80° C. during 5.5 hours, during which time the mixture became effervescent. The reaction mixture was cooled and poured slowly onto cracked ice. The resulting suspension was brought to pH 10 with solid potassium carbonate. Ice was added intermittently during this addition to maintain the temperature below 15° C. Toluene (150 ml) was added and the resulting mixture heated at 100° C. for one hour. The mixture was cooled and allowed to stand overnight. The two resulting layers were separated and the aqueous layer extracted with toluene (2×100 ml). The combined organic layers were washed with water (5×200 ml) and dried over anhydrous sodium sulfate. The solvent was evaporated in vacuo and the resulting yellow solid was triturated with hexane to yield 26 g of 2-(4-chlorophenyl)-3-dimethylaminopropenal as a tan solid mp. 120°-125° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726162
출처 데이터셋uspto-grants-1998_03
ORD IDord-8d9aaadeb71b457db37c796786d39ff2
출처 메모uspto-grants-1998_03