돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 415966생성일: 2026년 10월 25일

4-Amino-2-(trifluoromethyl)benzonitrile → N-(4-Cyano-3-trifluoromethyl-phenyl)-2-trifluoromethyl-acrylamide

https://huagongshe.com/reaction/415966

반응식

참여 물질

역할이름HCID투입량
반응물4-Amino-2-(trifluoromethyl)benzonitrileHCID 522170—
반응물2-(Trifluoromethyl)acrylic acidHCID 587694—
용매Diethyl EtherHCID 3283—
용매Thionyl ChlorideHCID 24386—
생성물N-(4-Cyano-3-trifluoromethyl-phenyl)-2-trifluoromethyl-acrylamideHCID 16756176—

반응 단계

2-Trifluoromethyl-acrylic acid (36.0 mmoL) in thionyl chloride (2.86 mL) was refluxed for 30 min. Excess thionyl chloride was removed in vacuo to yield a residue. 4-Amino-2-trifluoromethyl-benzonitrile (36.0 mmoL) in diethyl ether (50 mL) was added dropwise to the residue at −40° C. The reaction mixture was slowly warmed to room temperature. The reaction mixture was then partitioned between diethyl ether and water. The diethyl ether layer was washed with saturated sodium bicarbonate, then brine, dried over anhydrous Na2SO4, filtered and concentrated to yield a brown oil. The crude material (the brown oil) was then purified by column chromatography (silica gel, using ethyl acetate as eluent) to yield the title compound as yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088811B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-3551856c37c04845b183781b17b550da
출처 메모uspto-grants-2012_01