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Ammonium Hydroxide → 2-Amino-7-nitro-6-trifluoromethoxybenzothiazole

HRID 865794
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인쇄 미리보기

반응식

HRID 865794 반응식
Cl[C:2]1[S:3][C:4]2[C:10]([N+:11]([O-:13])=[O:12])=[C:9]([O:14][C:15]([F:18])([F:17])[F:16])[CH:8]=[CH:7][C:5]=2[N:6]=1.[OH-].[NH4+:20]>C(O)C>[NH2:20][C:2]1[S:3][C:4]2[C:10]([N+:11]([O-:13])=[O:12])=[C:9]([O:14][C:15]([F:18])([F:17])[F:16])[CH:8]=[CH:7][C:5]=2[N:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14923Ammonium HydroxideHCID 104700032-Chloro-7-nitro-6-trifluoromethoxybenzothiazole

생성물 1

HCID 99708192-Amino-7-nitro-6-trifluoromethoxybenzothiazole

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
110 °C

실험 절차

A mixture of 0.4 g of 2-chloro-7-nitro-6-trifluoromethoxybenzothiazole and 10 cm3 of 33% aqueous ammonium hydroxide solution in 30 cm3 of ethanol is heated at 110° C. in an autoclave for 5 hours. The mixture is cooled and the solvent is evaporated off under reduced pressure (2.7 kPa). After purification by flash chromatography on silica with a cyclohexane/ethyl acetate mixture (4/6 by volume) as eluent, 0.22 g of 2-amino-7-nitro-6-trifluoromethoxybenzothiazole is obtained, melting at 180° C.

후처리

  1. temperatureThe mixture is cooled
  2. customthe solvent is evaporated off under reduced pressure (2.7 kPa)
  3. customAfter purification by flash chromatography on silica with a cyclohexane/ethyl acetate mixture (4/6 by volume) as eluent

출처 및 근거

ORD 기록
ord-15785466c0fe416883f033db3706f711
출처 데이터셋
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05567822

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