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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38768생성일: 2026년 10월 24일

Dichloromethane → 4-{[2-Chloro-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}morpholine

https://huagongshe.com/ko/reaction/38768

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물MorpholineHCID 8083—
반응물TriethylamineHCID 8471—
반응물2-Chloro-4-(trifluoromethyl)pyrimidine-5-carbonyl chlorideHCID 2736708—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물4-{[2-Chloro-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}morpholineHCID 58168707—

반응 조건

온도-70 °C

반응 단계

A mixture of 2-chloro-4-(trifluoromethyl)pyrimidine-5-carbonyl chloride (2.8 g) and dichloromethane (56 mL) was cooled in a dry ice-acetone bath, and morpholine (990 μL) and triethylamine (1.9 mL) were added dropwise thereto while keeping the temperature at −50° C. or lower. The reaction mixture was stirred at −70° C. for 2.5 hours, and then ethyl acetate and water were added thereto. The aqueous layer was extracted with ethyl acetate, and the organic layer was washed with water and saturated brine. After drying over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain 4-{[2-chloro-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}morpholine (2.8 g) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524727B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-67953608ec5b4129a0de88b6f59f7c5b
출처 메모uspto-grants-2013_09