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HRID 62145作成日:2026年10月25日

Methyl Ethyl Ketone → 5-Bromo-2,3-dimethyl-1H-indole

https://huagongshe.com/reaction/62145

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl Ethyl KetoneHCID 6569—
反応物4-Bromophenylhydrazine hydrochlorideHCID 12157—
溶媒EthanolHCID 702—
生成物5-Bromo-2,3-dimethyl-1H-indoleHCID 1279309767%

反応手順

Following a published procedure (Gundersen, E. G. U.S. Patent App. Publ. US 2005/070592) 2-Butanone (0.11 mL, 1.278 mmol) was added to a solution of 4-bromophenylhydrazine hydrochloride (0.300 g, 1.342 mmol in EtOH (3.8 mL). The mixture was heated to reflux for 22 h, concentrated in vacuo, and partitioned between EtOAc and 1N HCl. The organic layer was washed with H2O and saturated aqueous NaHCO3, dried over Na2SO4, filtered, and concentrated. The crude residue was purified by chromatography (SiO2, 0-20% EtOAc/Hexane) to afford the desired indole as a pink powder (200 mg, 67%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09446022B2
出典データセットuspto-grants-2016_09
ORD IDord-fc7c7158f45b40b885208137dfb9ea7b
出典メモuspto-grants-2016_09