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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 380037생성일: 2026년 10월 27일

Hydrochloric Acid → 3-Bromo-5-trifluoromethylbenzenesulfonamide

https://huagongshe.com/reaction/380037

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sulfur DioxideHCID 1119—
반응물3-Bromo-5-(trifluoromethyl)anilineHCID 2735880—
반응물Magnesium ChlorideHCID 5360315—
반응물Sodium NitriteHCID 23668193—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물3-Bromo-5-trifluoromethylbenzenesulfonamideHCID 21895504—

반응 조건

온도-5 °C

반응 단계

3-Amino-5-bromobenzotrifluoride was added to concentrated hydrochloric acid (20 ml) and cooled to −5° C. A saturated solution of sodium nitrite (3.88 g) in water (4 ml) was dropwise added at such a rate to maintain the temperature below 0° C. Magnesium chloride (8 g) was added (CARE: exotherm) and the resulting mixture added with stirring to a saturated solution of sulfur dioxide in acetic acid (37.5 ml) and toluene (20 ml), containing cupric chloride (2.75 g) at room temperature. The mixture was stirred for 16 hours, poured into water and extracted into toluene. The combined toluene extracts were washed with water, dilute sodium hydrogen carbonate, dried over anhydrous magnesium sulfate and concentrated. The residue was dissolved in tetrahydrofuran (200 ml) and 880 ammonia (50 ml) was added to the solution. The mixture was stirred at room temperature for 4 hours and then concentrated under reduced pressure. The residue was partitioned between water and ethyl acetate. The combined ethyl acetate extracts were dried over anhydrous magnesium sulfate and concentrated to afford the sub-title compound as a solid (4.2 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300352B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-83fc3015a7f246068e62c58b29320cda
출처 메모uspto-grants-2001_10