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Methanol → 3-Fluoroquinolin-7-OL

HRID 454134
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HRID 454134 반응식
[F:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[C:7]([O:12]C)[CH:6]=2.B(Br)(Br)Br.CO>ClCCl>[F:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[C:7]([OH:12])[CH:6]=2
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참가 물질

5

반응물 3

HCID 887MethanolHCID 25134Boron tribromideHCID 220308563-Fluoro-7-methoxyquinoline

생성물 1

HCID 1357631243-Fluoroquinolin-7-OL

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

3-Fluoro-7-methoxyquinoline (130 mg, 0.74 mmol) was taken up in dichloromethane (2 ml) under nitrogen and treated with boron tribromide (4 ml of a 1.0M solution of in dichloromethane). The reaction mixture was stirred for 24 hours at ambient temperature followed by quenching the reaction by the slow addition of excess methanol. The solution was stirred for a further 2 hours and evaporated to dryness to give 3-fluoro-7-hydroxyquinoline which was used without further purification.

후처리

  1. customby quenching
  2. customthe reaction
  3. stirringThe solution was stirred for a further 2 hours
  4. customevaporated to dryness

출처 및 근거

ORD 기록
ord-9ecadf86ec4b4c428f8e3746328eae92
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08492560B2

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