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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 337612생성일: 2026년 10월 24일

Benzyl Bromide → 1-Benzyl-6-bromo-1H-indole-3-carbaldehyde

https://huagongshe.com/ko/reaction/337612

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Sodium hydrideHCID 24758—
반응물6-Bromoindole-3-carbaldehydeHCID 2794830—
용매DimethylformamideHCID 6228—
생성물1-Benzyl-6-bromo-1H-indole-3-carbaldehydeHCID 86651675—

반응 단계

6-Bromo-1H-indole-3-carbaldehyde (1 eq.) from the previous step was dissolved in DMF (0.19 M). Sodium hydride was added (1.5 eq.) and the resulting solution was stirred at RT for 20 min. Benzyl bromide (1 eq.) was then added and the reaction solution was allowed to stir at RT for 24 h. The reaction mixture was subsequently quenched with water and extracted with EtOAc. The combined organic extracts were dried over MgSO4. Filtration and concentration of the filtrate in vacuo afforded a yellow oil. Purification of the crude product thus obtained by way of flash chromatography (SiO2, 4:1 (v/v) Hex:EtOAc 3:7 (v/v) Hex:EtOAc) afforded the title compound as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889714B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-dc0bbd6d8f4346c5a4e4e1198226eb3d
출처 메모uspto-grants-2014_11