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Methanol → 3-Fluoroquinolin-7-OL

HRID 1791659
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HRID 1791659 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 11.0M 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-76e7e2024c9c4fb4b22242708b9a260b
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07074800B1

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