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Hydrogen Bromide → 1-Bromo-2-chloro-4-(trifluoromethoxy)benzene

HRID 266535
ノート
印刷プレビュー

反応式

HRID 266535 の反応式
N([O-])=O.[Na+].[Cl:5][C:6]1[CH:12]=[C:11]([O:13][C:14]([F:17])([F:16])[F:15])[CH:10]=[CH:9][C:7]=1N.[BrH:18]>S(=O)(=O)(O)O.C(O)(=O)C.O>[Cl:5][C:6]1[CH:12]=[C:11]([O:13][C:14]([F:17])([F:16])[F:15])[CH:10]=[CH:9][C:7]=1[Br:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 260Hydrogen BromideHCID 27340842-Chloro-4-(trifluoromethoxy)anilineHCID 23668193Sodium Nitrite

生成物 1

HCID 534140341-Bromo-2-chloro-4-(trifluoromethoxy)benzene

試薬・触媒・溶媒 3

HCID 176Acetic Acid溶媒HCID 962Water溶媒
HCID 1118
Sulfuric Acid
溶媒

実験手順

A solution of sodium nitrite (16.31 g) in concentrated sulphuric acid was added dropwise to a solution of 2-chloro-4-trifluoromethoxyaniline (50 g) in acetic acid, while maintaining the temperature below 10° C. The mixture was stirred at 5°-10° C. for 0.5 hours then added slowly to a mixture of cuprous bromide (33.9 g) in aqueous hydrobromic acid (200 ml) and ice. The mixture was stirred at room temperature for 0.5 hours and left to stand overnight. The mixture was diluted with water and extracted with dichloromethane, washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give 2-chloro-4-trifluoromethoxybromobenzene (63.64 g) as a brown oil which was not further purified.

後処理

  1. temperaturewhile maintaining the temperature below 10° C
  2. stirringThe mixture was stirred at room temperature for 0.5 hours
  3. waitleft
  4. waitto stand overnight
  5. extractionextracted with dichloromethane
  6. washwashed with water
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. customThe filtrate was evaporated to dryness

出典と根拠

ORDレコード
ord-d2d148276cd54858a13ee521177f5d16
出典データセット
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05650533

反応ノート

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