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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 745641생성일: 2026년 10월 24일

Tetrahydrofuran → [1alpha,3beta]-1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]androst-5-en-17-one

https://huagongshe.com/ko/reaction/745641

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물1-HydroxydehydroepiandrosteroneHCID 167955—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
용매DichloromethaneHCID 6344—
생성물[1alpha,3beta]-1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]androst-5-en-17-oneHCID 13189253—

반응 단계

A mixture of 0.91 g (0.0030 mol) of 1α,3β-dihydroxyandrost-5-en-17-one [R. M. Dodson, A. H. Goldkamp and R. D. Muir, J.Amer.Chem.Soc., 82, 4026 (1960)], 15 mL of tetrahydrofuran, 1.26 g (0.015 mol) of 3,4-dihydro-2H-pyran and 0.028 g of p-toluenesulfonic acid monohydrate was stirred at 25° for 18 hr. The mixture was diluted with methylene chloride. This solution was then washed with saturated aqueous sodium bicarbonate solution. The organic phase was dried over anhydrous magnesium sulfate, filtered and evaporated to dryness to yield oily [1α,3β]-1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]androst-5-en-17-one, [α]D20 +34.3° (c 1, CHCl3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04599330
출처 데이터셋uspto-grants-1986_07
ORD IDord-57c4f52724f54c2388446475f8e525ab
출처 메모uspto-grants-1986_07