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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37702생성일: 2026년 10월 24일

Ethyl-1-propyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-acetate → Ethyl-1-propyl-1,3,4,9-tetrahydro-6-hydroxypyrano[3,4-b]indole-1-acetate

https://huagongshe.com/ko/reaction/37702

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl-1-propyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-acetateHCID 19935728—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물Ethyl-1-propyl-1,3,4,9-tetrahydro-6-hydroxypyrano[3,4-b]indole-1-acetateHCID 1993574289.2%

반응 단계

A suspension of the 6-benzyloxypyranoindole (5.4 g, 13.25 mmol) of Step A, and 10% Pd/C catalyst (600 mg) in ethanol (150 mL) is hydrogenated for 6 hours in a Parr shaker. Filtration of the catalyst and evaporation of the solvent affords the title compound (3.75 g, 89%) as a cream-colored foam homogeneous by TLC.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420289
출처 데이터셋uspto-grants-1995_05
ORD IDord-85a7e5c46b2c42ea8680c7c2812bb776
출처 메모uspto-grants-1995_05