돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39222생성일: 2026년 10월 23일

Hydrochloric Acid → 2-Cyano-3-difluoromethoxyphenylsulfonyl chloride

https://huagongshe.com/ko/reaction/39222

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sulfur DioxideHCID 1119—
반응물Sodium NitriteHCID 23668193—
반응물2-Amino-6-difluoromethoxy-benzonitrileHCID 58100765—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물2-Cyano-3-difluoromethoxyphenylsulfonyl chlorideHCID 5810076791%

반응 조건

온도5 °C

반응 단계

2-Amino-6-difluoromethoxy-benzonitrile (6.4 g, 35 mmol) is dissolved in glacial acetic acid (50 ml). Hydrochloric acid (37%, 12.7 g) is added dropwise at ambient temperature. This mixture is cooled to 5° C. and a solution of sodium nitrite (2.5 g, 36.4 mmol) in Water (8 ml) is added dropwise. The reaction mixture is stirred at 0° C. for 1 hour. The resulting diazonium salt solution is added dropwise at ambient temperature to a mixture of glacial acetic acid (100 ml) saturated at ambient temperature with sulfur dioxide and a solution of CuCl2 (2.18 g, 16.2 mmol) in water (5 ml). The resulting mixture is stirred at ambient temperature for 2 hours. The reaction mixture is poured into an ice/water and extracted three times with dichloromethane. The combined organic phases are dried over sodium sulfate and concentrated to give 2-Cyano-3-difluoromethoxy-benzenesulfonyl chloride (8.5 g, 91% yield) which is used without further purification. 1H-NMR (CDCl3, 400 MHz): 8.10 (d, 1H), 7.85 (t, 1H), 7.75 (d, 1H), 6.75 (t, 1H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524896B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-8a94f41c9d4f4fdaa637af0309b079c2
출처 메모uspto-grants-2013_09