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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 508211생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/508211

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 번호US09095572B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-77877ed930054a36b291fe0f3c842203
출처 메모uspto-grants-2015_08