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Boron tribromide → 2-Chloro-6-hydroxyquinoline-3-carbaldehyde

HRID 1620208
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HRID 1620208 반응식
[Cl:1][C:2]1[C:11]([CH:12]=[O:13])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([O:14]C)[CH:8]=2)[N:3]=1.B(Br)(Br)Br>C(Cl)Cl>[Cl:1][C:2]1[C:11]([CH:12]=[O:13])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([OH:14])[CH:8]=2)[N:3]=1
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참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 6890792-Chloro-6-methoxyquinoline-3-carbaldehyde

생성물 1

HCID 210510652-Chloro-6-hydroxyquinoline-3-carbaldehyde수율 82%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 2-chloro-6-methoxyquinoline-3-carbaldehyde (1.01 g, 4.54 mmol) in dry CH2Cl2 (36 mL) in a 100 mL round-bottomed flask equipped with a magnetic stirrer at 0° C. under N2 was added dropwise BBr3 (1.0 N solution in CH2Cl2, 13.60 mL, 13.60 mmol). After complete addition, the bath was removed and stirring was continued overnight at RT. The reaction mixture was then added dropwise to a mixture of water and ice (50 mL) under stirring. After complete addition, the mixture was stirred for 30 min at RT and then filtered to give, after drying, 2-chloro-6-hydroxyquinoline-3-carbaldehyde as a yellow solid (0.77 g, 82% yield).

후처리

  1. additionAfter complete addition
  2. customthe bath was removed
  3. additionThe reaction mixture was then added dropwise to a mixture of water and ice (50 mL)
  4. stirringunder stirring
  5. additionAfter complete addition
  6. stirringthe mixture was stirred for 30 min at RT
  7. filtrationfiltered
  8. customto give
  9. customafter drying

출처 및 근거

ORD 기록
ord-c5ca210f7ff84ff4a081113922cd13e3
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772316B2

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