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

HRID 342977
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HRID 342977 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

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

생성물 1

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

시약·촉매·용매 3

HCID 176Acetic Acid용매HCID 962Water용매
HCID 1118
Sulfuric Acid
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-be70d093f5cd4d11af9348bb3408e6fd
출처 데이터셋
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05859283

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