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Methanol → 3-Fluoro-7-hydroxy-2-methylquinoline

HRID 454136
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HRID 454136 반응식
[F:1][C:2]1[C:3]([CH3:14])=[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[C:3]([CH3:14])=[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 220307923-Fluoro-7-methoxy-2-methylquinoline

생성물 1

HCID 1357631233-Fluoro-7-hydroxy-2-methylquinoline

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

3-Fluoro-7-methoxy-2-methylquinoline (0.16 g, 0.85 mmol) was taken up in dichloromethane (4 ml) under nitrogen and treated with boron tribromide solution (4 ml of a 1.0M solution in dichloromethane, 4.0 mmol). The reaction was stirred for 24 hours at ambient temperature followed by the slow addition of excess methanol. The solution was stirred for a further 2 hours and then evaporated to dryness to give 3-fluoro-7-hydroxy-2-methylquinoline which was used without further purification.

후처리

  1. stirringThe solution was stirred for a further 2 hours
  2. customevaporated to dryness

출처 및 근거

ORD 기록
ord-1671a113e0e84df59dd109665832c08a
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08492560B2

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