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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21701생성일: 2026년 10월 23일

6-(Trifluoromethoxy)-4-(trimethylsilyl)-2-benzothiazolamine → 6-Trifluoromethoxy-4-nitro-2-benzothiazolamine

https://huagongshe.com/ko/reaction/21701

반응식

참여 물질

역할이름HCID투입량
반응물6-(Trifluoromethoxy)-4-(trimethylsilyl)-2-benzothiazolamineHCID 9972441—
반응물Nitronium tetrafluoroborateHCID 11073463—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물6-Trifluoromethoxy-4-nitro-2-benzothiazolamineHCID 1177834643.3%

반응 조건

온도0 °C

반응 단계

0.68 g of nitronium tetrafluoroborate are added in small portions to a solution of 0.76 g of 2-amino-4-trimethylsilyl-6-trifluoromethoxybenzothiazole in 20 cm3 of acetonitrile cooled to 0° C. Stirring is continued for 12 hours at a temperature close to 20° C. The solution is then diluted with 50 cm3 of water and extracted with 2 times 50 cm3 of ethyl acetate. The organic phases are combined, dried over sodium sulphate and concentrated in vacuum. The residue is purified by flash chromatography on silica gel with a cyclohexane-ethyl acetate mixture (7-3 by volume) as eluent. After recrystallization from a cyclohexane-ethyl acetate mixture (3-2 by volume), 0.3 g of 2-amino-4-nitro-6-trifluoromethoxybenzothiazole melting at 260° C. is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424439
출처 데이터셋uspto-grants-1995_06
ORD IDord-3b531de0c67245a583860bb8674cac48
출처 메모uspto-grants-1995_06