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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 6-(Trifluoromethoxy)-4-(trimethylsilyl)-2-benzothiazolamine | HCID 9972441 | — |
| 반응물 | Nitronium tetrafluoroborate | HCID 11073463 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 6-Trifluoromethoxy-4-nitro-2-benzothiazolamine | HCID 11778346 | 43.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05424439 |
|---|
| 출처 데이터셋 | uspto-grants-1995_06 |
|---|
| ORD ID | ord-3b531de0c67245a583860bb8674cac48 |
|---|
| 출처 메모 | uspto-grants-1995_06 |
|---|