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Stannous Chloride → 4-Bromo-5-fluoro-1,2-benzenediamine

HRID 475210
ノート
印刷プレビュー

反応式

HRID 475210 の反応式
[Br:1][C:2]1[C:8]([F:9])=[CH:7][C:5]([NH2:6])=[C:4]([N+:10]([O-])=O)[CH:3]=1.Cl[Sn]Cl>CCO>[Br:1][C:2]1[CH:3]=[C:4]([NH2:10])[C:5]([NH2:6])=[CH:7][C:8]=1[F:9]
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 24479Stannous ChlorideHCID 219119284-Bromo-5-fluoro-2-nitroaniline

生成物 1

HCID 199585604-Bromo-5-fluoro-1,2-benzenediamine収率 43.4%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a suspension of 96 (1.57 g, 6.74 mmol) in EtOH (16 mL) was added SnCl2 (3.82 g, 20.2 mmol). The reaction mixture was heated at reflux for 14 h, cooled to RT and concentrated in vacuo. The residue was partitioned between EtOAc (100 mL) and sat'd. aq. NaHCO3 (200 mL). The resulting slurry was filtered through a pad of Celite® and the wet cake was washed with EtOAc (3×50 mL). The organic layer was washed sequentially with saturated NaHCO3, water, and brine, dried (MgSO4), filtered and concentrated in vacuo to afford 600 mg (43%) of 4-bromo-5-fluorobenzene-1,2-diamine (98) as yellow solid: MS (ESI) m/z=205 [M+1]+.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 14 h
  3. concentrationconcentrated in vacuo
  4. customThe residue was partitioned between EtOAc (100 mL)
  5. filtrationThe resulting slurry was filtered through a pad of Celite®
  6. washthe wet cake was washed with EtOAc (3×50 mL)
  7. washThe organic layer was washed sequentially with saturated NaHCO3, water, and brine
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-7a9c016805e44a2d9e54cc9d32800f67
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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