Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → [1alpha,3beta]-1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]androst-5-en-17-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| 반응물 | 1-Hydroxydehydroepiandrosterone | HCID 167955 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | [1alpha,3beta]-1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]androst-5-en-17-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04599330 |
| 출처 데이터셋 | uspto-grants-1986_07 |
| ORD ID | ord-57c4f52724f54c2388446475f8e525ab |
| 출처 메모 | uspto-grants-1986_07 |