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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37700생성일: 2026년 10월 23일

p-Toluenesulfonic acid → 1-Methyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-aceticacid, ethyl ester

https://huagongshe.com/ko/reaction/37700

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Ethyl AcetoacetateHCID 8868—
반응물5-Benzyloxy-3-(2-hydroxyethyl)indoleHCID 744849—
용매BenzeneHCID 241—
생성물1-Methyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-aceticacid, ethyl esterHCID 13171802985.3%

반응 단계

A mixture consisting of 5-benzyloxytryptophol (4.5 g, 0.017 mol), benzene (200 mL), ethyl acetoacetate (3.4 g, 0.026 mol) and p-toluenesulfonic acid (0.5 g) is refluxed for 2.5 hours using a Dean-stock trap to remove the water. The reaction mixture is cooled to room temperature and washed with 5% sodium bicarbonate, (1×200 mL), water (200 mL) and brine (100 mL), dried (MgSO4), filtered and concentrated to give 8.0 g of crude product as a thick oil, which is flash chromatographed on silica gel using 20% ethyl acetate/hexane as an eluent to afford 5.5 g oil which solidifies upon standing, m.p. 96°-98° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420289
출처 데이터셋uspto-grants-1995_05
ORD IDord-0c87532d6195447a8d6305239c03c6aa
출처 메모uspto-grants-1995_05