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Hydrogen Bromide → 1-Bromo-3-isobutylbenzene

HRID 1034048
ノート
印刷プレビュー

反応式

HRID 1034048 の反応式
[CH2:1]([C:5]1[CH:6]=[C:7](N)[CH:8]=[CH:9][CH:10]=1)[CH:2]([CH3:4])[CH3:3].N([O-])=O.[Na+].[BrH:16]>>[Br:16][C:7]1[CH:8]=[CH:9][CH:10]=[C:5]([CH2:1][CH:2]([CH3:4])[CH3:3])[CH:6]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 260Hydrogen Bromide2 回HCID 190247993-IsobutylanilineHCID 23668193Sodium Nitrite

生成物 1

HCID 187549911-Bromo-3-isobutylbenzene

反応条件

温度
25 °C

実験手順

To a solution of 3-isobutylphenylamine (3.80 g) in 48% hydrobromic acid (10 ml) was added aqueous sodium nitrite (2.11 g, 2 ml) below 10° C. over 20 minutes. The reaction mixture was added to a solution of cuprous bromide (7.3 g) in 48% hydrobromic acid(5 ml) at 25° C. After stirred at 25° C. for 1 hour, the mixture was extracted with hexane two times. The extracts were combined, washed with water and brine, and dried over magnesium sulfate. After evaporation of the solvent, the residue was chromatographed on silica gel (150 g) eluting with hexane to give 1-bromo-3-isobutylbenzene (2.61 g) as a colorless oil.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. extractionthe mixture was extracted with hexane two times
  2. washwashed with water and brine
  3. dry with materialdried over magnesium sulfate
  4. customAfter evaporation of the solvent
  5. customthe residue was chromatographed on silica gel (150 g)
  6. washeluting with hexane

出典と根拠

ORDレコード
ord-699d5d0ad31d4e5f8c37746571dd7d28
出典データセット
uspto-grants-1994_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05312829

反応ノート

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