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Stannous Chloride → Methyl 3-amino-5-(trifluoromethyl)benzoate

HRID 355368
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HRID 355368 반응식
[Sn](Cl)Cl.[N+:4]([C:7]1[CH:8]=[C:9]([CH:14]=[C:15]([C:17]([F:20])([F:19])[F:18])[CH:16]=1)[C:10]([O:12][CH3:13])=[O:11])([O-])=O>C(O)C>[NH2:4][C:7]1[CH:8]=[C:9]([CH:14]=[C:15]([C:17]([F:18])([F:19])[F:20])[CH:16]=1)[C:10]([O:12][CH3:13])=[O:11]
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참가 물질

4

반응물 2

HCID 24479Stannous ChlorideHCID 18942157Methyl 3-nitro-5-(trifluoromethyl)benzoate

생성물 1

HCID 4026781Methyl 3-amino-5-(trifluoromethyl)benzoate수율 56.6%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
60 °C

실험 절차

Tin (II) chloride (60 g) was added to a solution of methyl 3-nitro-5-(trifluoromethyl)benzoate (25 g, 100 mmol) in ethanol (600 ml) and the mixture was heated to 60° C. for 2 hours. The mixture was cooled and concentrated under reduced pressure to approximately one third volume. The mixture was added slowly to saturated aqueous sodium hydrogen carbonate (1000 ml) and the resulting mixture was filtered through celite. The filter cake was washed with ethyl acetate (500 ml). The organic layer was dried (MgSO4) and the solvent was evaporated under reduced pressure to give methyl 3-amino-5-(trifluoromethyl)benzoate as an orange solid (12.4 g), 1H NMR (360 MHz,CDCl3) δ 3.95 (3H, s), 7.08 (1H, br s), 7.51 (1H, s), and 7.66 (1H, s).

후처리

  1. temperatureThe mixture was cooled
  2. concentrationconcentrated under reduced pressure to approximately one third volume
  3. additionThe mixture was added slowly to saturated aqueous sodium hydrogen carbonate (1000 ml)
  4. filtrationthe resulting mixture was filtered through celite
  5. washThe filter cake was washed with ethyl acetate (500 ml)
  6. dry with materialThe organic layer was dried (MgSO4)
  7. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-0f6c6afc452a428e8393c6ce38f31fd0
출처 데이터셋
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05830892

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