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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 334433생성일: 2026년 10월 24일

Trichloroacetic Acid → 2,2,2-Trichloro-1-(4-(4-methylpiperazine-1-yl)phenyl)ethanol

https://huagongshe.com/ko/reaction/334433

반응식

참여 물질

역할이름HCID투입량
반응물Trichloroacetic AcidHCID 6421—
반응물4-(4-Methylpiperazin-1-yl)benzaldehydeHCID 736533—
반응물Sodium TrichloroacetateHCID 23681045—
용매DimethylformamideHCID 6228—
생성물2,2,2-Trichloro-1-(4-(4-methylpiperazine-1-yl)phenyl)ethanolHCID 6827717282%

반응 단계

1.0 ml (10.00 mmol) of trichloroacetic acid and, in small portions, 1.854 g. (10 mmol) of sodium 2,2,2-trichloroacetate are added at room temperature to a solution of 1.362 g (6.67 mmol) of 4-(4-methylpiperazine-1-yl)benzaldehyde in 13.5 ml of dimethylformamide. The reaction mixture is stirred for 3 hours at room temperature. The solvent is concentrated and the crude reaction product extracted with ethyl acetate. The organic phase is washed using saturated sodium bicarbonate solution. The organic phases are combined, dried on magnesium sulfate and then concentrated to yield 1.760 g (yield=82%) of 2,2,2-trichloro-1-(4-(4-methylpiperazine-1-yl)phenyl)ethanol in the form of a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883821B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-515ca87369a043708f8648e14abc16e2
출처 메모uspto-grants-2014_11