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Stannous Chloride → 3-Bromobenzene-1,2-diamine

HRID 475106
ノート
印刷プレビュー

反応式

HRID 475106 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([N+:8]([O-])=O)[C:3]=1[NH2:11].Cl[Sn]Cl>CCO>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([NH2:8])[C:3]=1[NH2:11]
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 114699892-Bromo-6-nitroaniline

生成物 1

HCID 124898393-Bromobenzene-1,2-diamine収率 90%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A suspension of 2-bromo-6-nitrobenzenamine (2.0 g, 9 mmol) and SnCl2 (10.2 g, 54 mmol) in EtOH (20 mL) was heated at reflux for 2 h, then cooled to RT and concentrated in vacuo. The residue was diluted with EtOAc (100 mL) and washed with saturated NaHCO3 solution (200 mL). The resulting slurry was filtered through a pad of Celite® and washed with EtOAc (50 ml, ×3). The filtrate was washed with saturated NaHCO3, water, and brine, dried (MgSO4), filtered and concentrated in vacuo to afford 3-bromobenzene-1,2-diamine as a brown oil (1.5 g, 90%). MS (ESI): m/z=186.9 [M+1]+.

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 2 h
  3. concentrationconcentrated in vacuo
  4. additionThe residue was diluted with EtOAc (100 mL)
  5. washwashed with saturated NaHCO3 solution (200 mL)
  6. filtrationThe resulting slurry was filtered through a pad of Celite®
  7. washwashed with EtOAc (50 ml, ×3)
  8. washThe filtrate was washed with saturated NaHCO3, water, and brine
  9. dry with materialdried (MgSO4)
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-50415e52d9c643df8d1432bd69692235
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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