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Stannous chloride dihydrate → 4-Bromo-3-fluorobenzene-1,2-diamine

HRID 475226
ノート
印刷プレビュー

反応式

HRID 475226 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[C:4]([N+:9]([O-])=O)[C:3]=1[F:12].O.O.Cl[Sn]Cl>CCO>[Br:1][C:2]1[C:3]([F:12])=[C:4]([NH2:9])[C:5]([NH2:8])=[CH:6][CH:7]=1
参加物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 61436Stannous chloride dihydrateHCID 27831584-bromo-3-fluoro-2-nitroaniline

生成物 1

HCID 27832034-Bromo-3-fluorobenzene-1,2-diamine収率 84.7%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of 140 (34 g, 0.144 mol) and EtOH (510 mL) was added SnCl2.2H2O (130.1 g, 0.576 mol) and the resulting mixture was heated to reflux for 4 h. After the completion of the reaction, the solvent was removed in vacuo. The residue was taken up in water and made slightly basic with 10% NaHCO3. The resulting solid was filtered and washed well with EtOAc. The aqueous layer was separated and extracted with EtOAc. The combined organic layers were dried (Na2SO4), filtered and concentrated in vacuo to afford 25 g (84%) of 4-bromo-3-fluoro-benzene-1,2-diamine (142) as yellow solid which was used without further purification.

後処理

  1. temperaturethe resulting mixture was heated
  2. temperatureto reflux for 4 h
  3. customAfter the completion of the reaction
  4. customthe solvent was removed in vacuo
  5. filtrationThe resulting solid was filtered
  6. washwashed well with EtOAc
  7. customThe aqueous layer was separated
  8. extractionextracted with EtOAc
  9. dry with materialThe combined organic layers were dried (Na2SO4)
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-593ca89e47be4721987adce82fd9c07d
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08637537B2

反応ノート

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