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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30890생성일: 2026년 10월 24일

Sulfuryl chloride → 2-Chloro-5-(trifluoromethyl)-1,3-benzothiazole

https://huagongshe.com/ko/reaction/30890

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuryl chlorideHCID 24648—
반응물5-(trifluoromethyl)-1,3-benzothiazole-2-thiolHCID 178419087—
생성물2-Chloro-5-(trifluoromethyl)-1,3-benzothiazoleHCID 2198584994%

반응 단계

Sulfuryl chloride (9.09 g, 67.33 mmol) was added with stirring to 2-mercapto-5-(trifluoromethyl)benzothiazole (2.64 g, 11.22 mmol) over a period of 5 minutes. The reaction mixture was then allowed to stand for approximately 1 h. Ice water was added to the reaction mixture with stirring to decompose the excess of sulfuryl chloride, and the product was then extracted with ethyl acetate. The organic layer was washed with water (3×) and brine, dried over anhydrous Na2SO4 and concentrated. The resulting solid was dissolved in EtOAc and filtered though a short silica-gel column, eluting with EtOAc, to give 2-chloro-5-(trifluoromethyl)benzothiazole (2.50 g, 94%). LC-MS m/z 238.0 (MH+), ret. time 2.55 min; 1H NMR (400 MHz, DMSO-d6) δ 7.81 (d, 1H), 8.38 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423156B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-921fd12bd97a499788225f411c64e142
출처 메모uspto-grants-2008_09