Ethanol → Benzenamine, 2-bromo-5-chloro-3-methyl-

HRID 2216053ノート

反応式

HRID 2216053 の反応式
[Br:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][C:5]([Cl:11])=[CH:4][C:3]=1[CH3:12].CCO.[Cl-].[NH4+]>[Fe].O>[Br:1][C:2]1[C:3]([CH3:12])=[CH:4][C:5]([Cl:11])=[CH:6][C:7]=1[NH2:8]

参加物

6

反応条件

温度
50 °C

実験手順

2-Bromo-5-chloro-1-methyl-3-nitro-benzene (721 mg, 3.5 mmol, Example 135: step b) was dissolved into EtOH (6 mL). To this was added ammonium chloride (1.9 g, 35 mmol) dissolved into water (10 mL). The reaction was heated to 50° C., iron (9.6 mg, 0.34 mmol) was added and the reaction was then heated to 80° C. for 12 hours. The reaction mixture was filtered through celite, washed with methanol and EtOAc and the solvents were removed in vacuo. The residue was dissolved into EtOAc and washed with brine to remove salts. The organic layers were dried (MgSO4) and the solvents were removed in vacuo resulting in the title compound (595 mg, 78%) as a brown solid. 1H-NMR (CDCl3): δ 6.63–6.61 (m, 2H), 2.33 (s, 3H).

後処理

  1. temperaturethe reaction was then heated to 80° C. for 12 hours
  2. filtrationThe reaction mixture was filtered through celite
  3. washwashed with methanol and EtOAc
  4. customthe solvents were removed in vacuo
  5. dissolutionThe residue was dissolved into EtOAc
  6. washwashed with brine
  7. customto remove salts
  8. dry with materialThe organic layers were dried (MgSO4)
  9. customthe solvents were removed in vacuo

出典と根拠

ORDレコード
ord-b6569502b5904de7b79cf5f1dd49162f
出典データセット
uspto-grants-2006_09
特許番号
US07109354B2

反応ノート

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