Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Amino-2-(trifluoromethyl)benzonitrile → N-(4-Cyano-3-trifluoromethyl-phenyl)-2-trifluoromethyl-acrylamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Amino-2-(trifluoromethyl)benzonitrile | HCID 522170 | — |
| 반응물 | 2-(Trifluoromethyl)acrylic acid | HCID 587694 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Thionyl Chloride | HCID 24386 | — |
| 생성물 | N-(4-Cyano-3-trifluoromethyl-phenyl)-2-trifluoromethyl-acrylamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08088811B2 |
| 출처 데이터셋 | uspto-grants-2012_01 |
| ORD ID | ord-3551856c37c04845b183781b17b550da |
| 출처 메모 | uspto-grants-2012_01 |