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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2046654생성일: 2026년 10월 26일

Water → 2-Chloro-4,5-difluorobenzonitrile

https://huagongshe.com/reaction/2046654

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PyridineHCID 1049—
반응물Oxalyl chlorideHCID 65578—
반응물2-Chloro-4,5-difluorobenzamideHCID 2317151—
용매DimethylformamideHCID 6228—
생성물2-Chloro-4,5-difluorobenzonitrileHCID 408584992%

반응 단계

To a solution (20 mL) of 2-chloro-4,5-difluorobenzoic acid (1.0 g) in N,N-dimethylformamide were added N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (1.15 g) and N-hydroxysuccinimide (717 mg) under ice-cooling, and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added 28% aqueous ammonia solution (2 mL) under ice-cooling, and the mixture was stirred at room temperature for 30 min. Water was added to the mixture and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 2-chloro-4,5-difluorobenzamide as a colorless solid (yield: 760 mg, yield: 76%). To a solution (5 mL) of 2-chloro-4,5-difluorobenzamide (300 mg) in N,N-dimethylformamide was added pyridine (0.253 mL), and oxalyl chloride (0.20 mL) was added dropwise thereto under ice-cooling. The reaction mixture was stirred at room temperature for 30 min, water was added to the mixture and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound as a colorless solid (yield: 250 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08592452B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-023c75c9557244659fec8c691815ae6f
출처 메모uspto-grants-2013_11