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Ammonium Chloride → Benzenamine, ar-bromo-ar-chloro-

HRID 1043703
ノート
印刷プレビュー

反応式

HRID 1043703 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([N+:8]([O-])=O)[C:3]=1[Cl:11].[NH4+].[Cl-]>CO.[Zn]>[Br:1][C:2]1[C:3]([Cl:11])=[C:4]([CH:5]=[CH:6][CH:7]=1)[NH2:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 25517Ammonium ChlorideHCID 227360531-Bromo-2-chloro-3-nitrobenzene

生成物 1

HCID 189585Benzenamine, ar-bromo-ar-chloro-収率 82.7%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 887Methanol溶媒

実験手順

To a solution of 1-bromo-2-chloro-3-nitrobenzene (3.0 g, 12.7 mmol) in MeOH (127 ml) was added Zn dust (8.30 g, 127 mmol) followed by NH4Cl (6.79 g, 127 mmol) which resulted in a significant exotherm. The heterogeneous reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was filtered through a pad of Celite and concentrated to an off-white solid. To this solid was added EtOAc and the resulting mixture was sonicated for 10 minutes. The mixture was filtered through Celite and washed with EtOAc. The combine filtrates were concentrated in vacuo to afford 2.17 g (10.5 mmol, 79%) of 3-bromo-2-chloroaniline: LCMS (m/z): 205.9 (MH+); tR=0.87 minute: 1H NMR (400 MHz, CDCl3) δ 6.62-6.66 (m, 1H) 6.87 (t, J=8.0 Hz, 1H) 6.97 (d, J=7.8 Hz, 1H) 7.22 (d, J=9.0 Hz, 1H).

後処理

  1. customresulted in a significant exotherm
  2. filtrationThe reaction mixture was filtered through a pad of Celite
  3. concentrationconcentrated to an off-white solid
  4. additionTo this solid was added EtOAc
  5. customthe resulting mixture was sonicated for 10 minutes
  6. filtrationThe mixture was filtered through Celite
  7. washwashed with EtOAc
  8. concentrationThe combine filtrates were concentrated in vacuo

出典と根拠

ORDレコード
ord-70eb5018e6f849c99796a53a5e1802db
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08563553B2

反応ノート

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