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Water → 5-Chloro-3-(trifluoromethyl)benzene-1,2-diamine

HRID 53766
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HRID 53766 반응식
[NH2:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][C:5]([Cl:11])=[CH:4][C:3]=1[C:12]([F:15])([F:14])[F:13].Cl[Sn]Cl.O>C(O)C>[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][C:5]([Cl:11])=[CH:4][C:3]=1[C:12]([F:15])([F:13])[F:14]
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참가 물질

5

반응물 3

HCID 962WaterHCID 24479Stannous ChlorideHCID 27376442-Amino-5-chloro-3-nitrobenzotrifluoride

생성물 1

HCID 27734985-Chloro-3-(trifluoromethyl)benzene-1,2-diamine수율 83%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
90 °C

실험 절차

To a stirred mixture of 2-amino-5-chloro-3-nitrobenzotrifluoride (250 mg, 1.043 mmol) in ethanol (4 mL) was added SnCl2.2 H2O (1.174 g, 5.217 mmol) in one portion. The mixture was refluxed at 80° C. (oil bath 90° C.) for 1 h. The solution was cooled to room temperature and ice water (20 g) was added. It was adjusted to pH=7 and extracted with ethyl acetate. The extract was dried (Mg2SO4) and evaporated to give 181 mg (83%) of 2,3-diamino-5-chlorobenzotrifluoride as a brown solid. 1H NMR (CDCl3): δ 3.515 (s, 2H); 3.878 (s, 2H); 6.845 (s, 1H); 6.988 (s, 1H).

후처리

  1. temperatureThe solution was cooled to room temperature
  2. extractionextracted with ethyl acetate
  3. dry with materialThe extract was dried (Mg2SO4)
  4. customevaporated

출처 및 근거

ORD 기록
ord-8f3dd66af05a47d78c924dd9dc267382
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05620979

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