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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 489997생성일: 2026년 10월 24일

N,N-Dimethylbenzamide → 4'-(Trifluoromethyl)-[1,1'-biphenyl]-2-carbonyl chloride

https://huagongshe.com/ko/reaction/489997

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylbenzamideHCID 11916—
반응물Thionyl ChlorideHCID 24386—
반응물4'-(Trifluoromethyl)(1,1'-biphenyl)-2-carboxylic acidHCID 55251—
용매TolueneHCID 1140—
생성물4'-(Trifluoromethyl)-[1,1'-biphenyl]-2-carbonyl chlorideHCID 11066000—

반응 조건

온도80 °C

반응 단계

Alternative A. 4′-(Trifluoromethyl)[1,1′-biphenyl]-2-carboxylic acid (133 g), commercially available, thionyl chloride (89 g) and a catalytic amount of N,N-dimethylbenzamide (2.3 g) were combined in toluene (665 mL) at 55-60° C. over 2 hours, and the mixture heated at 80° C. for 1 hour. The excess reagent was removed by atmospheric co-distillation with toluene (600 ml distillate removed), providing a solution of 4′-(trifluoromethyl)[1,1′-biphenyl]-2-carbonyl chloride, which was combined with ethyl 5-amino-1-methyl-1H-indole-2-carboxylate (109 g) from the previous step, ethyl acetate (4660 ml) and N,N-diisopropylethylamine (131 mL) at 18-29° C. The resulting slurry was cooled, filtered and the crude product solids were washed with propan-2-ol (330 mL). The crude product was twice reslurried in a 70/30 mixture of demineralized water and propan-2-ol (2×1500 mL), and the solids were filtered, washed with propan-2-ol (400 mL) and dried, yielding the title compound, ethyl 1-methyl-5-[4′-(trifluoromethyl)[1,1′-biphenyl]-2-carboxamido]-1H-indole-2-carboxylate (167 g, 71.8%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06979692B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-554fb68af22240c8bb73c61d0251a485
출처 메모uspto-grants-2005_12