Aluminum(III) Chloride → 6-Bromo-7-chloro-3,4-dihydroquinolin-2(1H)-one

HRID 1774833노트

반응식

HRID 1774833 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9](=[O:13])[CH2:10][CH2:11]Cl)=[CH:4][C:3]=1[Cl:14].[Cl-].[Al+3].[Cl-].[Cl-]>>[Br:1][C:2]1[CH:7]=[C:6]2[C:5](=[CH:4][C:3]=1[Cl:14])[NH:8][C:9](=[O:13])[CH2:10][CH2:11]2

참가 물질

3

반응물 2

HCID 6451240Aluminum(III) ChlorideHCID 86679184N-(4-bromo-3-chloro-phenyl)-3-chloro-propionamide

생성물 1

HCID 709793626-Bromo-7-chloro-3,4-dihydroquinolin-2(1H)-one수율 50.3%

실험 절차

A flame-dried 50-mL flask equipped with a magnetic stirring bar was charged with N-(4-bromo-3-chloro-phenyl)-3-chloro-propionamide (1.0 g, 3.36 mmol) and aluminium chloride (0.67 g, 5.04 mmol). In a pre-heated oil bath, the flask was heated at 135˜140° C. for 2 hours. After cooling to room temperature, the reaction mixture was treated slowly with ice-water, then extracted with EtOAc. The organic layer was washed with water and brine in sequence and dried over anhydrous Na2SO4. After evaporation of the solvent, the residue was purified by recrystallization from EtOAc (2 mL) which gave title compound (0.44 g, 50%) as a solid. MS: 260.0 (M+H+)+.

후처리

  1. customA flame-dried 50-mL flask equipped with a magnetic stirring bar
  2. temperatureIn a pre-heated oil bath, the flask was heated at 135˜140° C. for 2 hours
  3. extractionextracted with EtOAc
  4. washThe organic layer was washed with water and brine in sequence
  5. dry with materialdried over anhydrous Na2SO4
  6. customAfter evaporation of the solvent
  7. customthe residue was purified by recrystallization from EtOAc (2 mL) which

출처 및 근거

ORD 기록
ord-21fb40fc4a674337b121db420117bb32
출처 데이터셋
uspto-grants-2016_02
특허 번호
US09260408B2

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