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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490811생성일: 2026년 10월 25일

Methyl iodide → 4-(Benzyloxy)-1-methyl-1H-indole

https://huagongshe.com/reaction/490811

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물4-(phenylmethoxy)-1H-indoleHCID 88465—
생성물4-(Benzyloxy)-1-methyl-1H-indoleHCID 24776901—

반응 단계

Compounds of Formula I can be prepared as illustrated by exemplary reaction in Scheme 1. Reaction of 4-benzyloxy-indole with MeI in the presence of a base such as NaH produced 4-benzyloxy-1-methyl-indole. The benzyl protecting group was removed by hydrogenation to give the 4-hydroxy-1-methyl-indole. Reaction of 4-hydroxy-1-methyl-indole with an aryl-aldehyde such as 5-bromoveratraldehyde and malononitrile in the presence of a base such as piperidine produced the substituted 7-methyl-pyrrolo[2,3-h]chromene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528164B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-df73c1e276a34e649959f5acc7ef1727
출처 메모uspto-grants-2009_05