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

HRID 355368
ノート
印刷プレビュー

反応式

HRID 355368 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
60 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-0f6c6afc452a428e8393c6ce38f31fd0
出典データセット
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05830892

反応ノート

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