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HRID 62145생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/62145

반응식

참여 물질

역할이름HCID투입량
반응물Methyl Ethyl KetoneHCID 6569—
반응물4-Bromophenylhydrazine hydrochlorideHCID 12157—
용매EthanolHCID 702—
생성물5-Bromo-2,3-dimethyl-1H-indoleHCID 1279309767%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09446022B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-fc7c7158f45b40b885208137dfb9ea7b
출처 메모uspto-grants-2016_09