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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37705생성일: 2026년 10월 24일

p-Toluenesulfonic acid → 1,3,4,9-Tetrahydro-1,1-diethyl-6-(phenylmethoxy)pyrano[3,4-b]indole

https://huagongshe.com/ko/reaction/37705

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Ethyl ketoneHCID 7288—
반응물5-Benzyloxy-3-(2-hydroxyethyl)indoleHCID 744849—
용매BenzeneHCID 241—
생성물1,3,4,9-Tetrahydro-1,1-diethyl-6-(phenylmethoxy)pyrano[3,4-b]indoleHCID 19935702—

반응 단계

A mixture consisting of 5-benzyloxytryptophol (7.0 g, 0.0262 mol), diethyl ketone (10 mL), benzene (400 mL) and p-toluene sulfonic acid is refluxed for 3.5 hours using a Dean-Stark tap to remove the water. The reaction mixture is cooled to room temperature, washed with 5% sodium bicarbonate, water (200 mL), brine (200 mL), dried (MgSO4), filtered and concentrated to give 9.9 g of crude product. The crude product is flash chromatographed on silica gel using 15% ethyl acetate/hexane as an eluent to afford 6.5 g of pure title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420289
출처 데이터셋uspto-grants-1995_05
ORD IDord-a09d1d9c3a1d4cbca6ef532f7dd1bb33
출처 메모uspto-grants-1995_05