Boron tribromide → 4-fluoro-2-methyl-1H-indol-5-ol
反応式
[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]2参加物
4
実験手順
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%).
後処理
- additionthe mixture was poured onto water
- customThe organic layer was separated
- washwashed with water, brine
- dry with materialdried (MgSO4)
- customevaporated
- customThe residue was purified by column chromatography
- washeluting with ethyl acetate/petroleum ether (3/7)
出典と根拠
- ORDレコード
- ord-3a3732b9bc3a4e508995ad8b51078eb8
- 出典データセット
- uspto-grants-2006_07
- 特許番号
- US07074800B1
反応ノート
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