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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423360생성일: 2026년 10월 23일

Iodoform → 4-Carboxy-2-iodobenzotrifluoride, 3-Iodo-alpha,alpha,alpha-trifluoro-p-toluic acid

https://huagongshe.com/ko/reaction/423360

반응식

참여 물질

역할이름HCID투입량
반응물IodoformHCID 6374—
반응물Butyl nitriteHCID 10996—
반응물3-Amino-4-(trifluoromethyl)benzoic acidHCID 642651—
용매TetrahydrofuranHCID 8028—
생성물4-Carboxy-2-iodobenzotrifluoride, 3-Iodo-alpha,alpha,alpha-trifluoro-p-toluic acidHCID 59318424—

반응 조건

온도80 °C

반응 단계

3-Amino-4-(trifluoromethyl)benzoic acid (commercially available) (6.5 g, 31.7 mmol) and triiodomethane (37.4 g, 95.1 mmol) were dissolved in THF (300 ml). The reaction mixture was heated to 80° C. and then butyl nitrite (5.56 ml, 47.6 mmol) was added slowly at this temperature. Heating was continued at this temperature for 4 hours and then the reaction was concentrated in vacuo to give the crude product. Purification by column chromatography (hexane to 30% EtOAc in hexane). This material was combined with another batch from a similar reaction performed on 2 g of 3-amino-4-(trifluoromethyl)benzoic acid. The combined material was purified by preparative HPLC to give the title compound (6.1 g). MS C8H4F3IO2 requires 316; found 315 (M−H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101775B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-8c22aa50f5d6404d9219efda24c2f897
출처 메모uspto-grants-2012_01