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Boron tribromide → 4-fluoro-2-methyl-1H-indol-5-ol

HRID 454215
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HRID 454215 반응식
[F:1][C:2]1[C:10]([O:11]C)=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH3:13])[NH:6]2.B(Br)(Br)Br>C(Cl)Cl>[F:1][C:2]1[C:10]([OH:11])=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH3:13])[NH:6]2
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참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 220307284-Fluoro-5-methoxy-2-methyl-1H-indole

생성물 1

HCID 103520364-fluoro-2-methyl-1H-indol-5-ol수율 70.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

To a solution of 4-fluoro-5-methoxy-2-methylindole (709 mg, 3.95 mmol) in methylene chloride (9 ml) cooled at −30° C. was added a solution of boron tribromide (2.18 g, 8.7 mmol) in methylene chloride (1 ml). After stirring for 1 hour at ambient temperature, the mixture was poured onto water and was diluted with methylene chloride. The pH of the aqueous layer was adjusted to 6. The organic layer was separated, washed with water, brine, dried (MgSO4) and evaporated. The residue was purified by column chromatography, eluting with ethyl acetate/petroleum ether (3/7) to give 4-fluoro-5-hydroxy-2-methylindole (461 mg, 70%).

후처리

  1. additionthe mixture was poured onto water
  2. customThe organic layer was separated
  3. washwashed with water, brine
  4. dry with materialdried (MgSO4)
  5. customevaporated
  6. customThe residue was purified by column chromatography
  7. washeluting with ethyl acetate/petroleum ether (3/7)

출처 및 근거

ORD 기록
ord-3b41a90ffadc414ca57f84b47f4d2294
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08492560B2

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