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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430773생성일: 2026년 10월 24일

Benzyl Bromide → 4-(phenylmethoxy)-1H-indole

https://huagongshe.com/ko/reaction/430773

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium HydroxideHCID 14797—
반응물1H-indol-4-olHCID 75421—
용매DimethylformamideHCID 6228—
생성물4-(phenylmethoxy)-1H-indoleHCID 8846585%

반응 단계

Potassium hydroxide (0.42 g) was added to 4-hydroxyindole (1.00 g) in DMF (25 ml), and the solution was stirred at room temperature for 15 minutes. Benzyl bromide (1.00 ml) was added to the solution, and the solution was stirred at room temperature for 1.5 hours. Since the reaction was not completed, benzyl bromide (0.20 ml) was further added and the solution was stirred for 5 hours. After removing the solvent under reduced pressure, water (50 ml) was added to the residue and the resultant was extracted with ether (3×50 ml). The organic layers were washed with saturated brine, and dried over sodium sulfate. After removing solids by filtration, the solvent was removed under reduced pressure and the obtained crude product was purified by silica gel column chromatography to obtain the desired product (1.43 g, yield: 85%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06323235B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-ded0112ca83f4afa952d72e5c70ce665
출처 메모uspto-grants-2001_11