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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329535생성일: 2026년 10월 25일

Water → 1alpha,3beta-Bis(triethylsilyloxy)-5-androsten-17-one

https://huagongshe.com/reaction/329535

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물ChlorotriethylsilaneHCID 13819—
반응물1-HydroxydehydroepiandrosteroneHCID 167955—
용매PyridineHCID 1049—
생성물1alpha,3beta-Bis(triethylsilyloxy)-5-androsten-17-oneHCID 13985469—

반응 단계

In 600 ml of pyridine, 9.13 g of 1α-hydroxydehydroepiandrosterone was suspended. Under an argon stream, 100 ml of triethylamine and 39.0 g of triethyl chlorosilane were added to the suspension, and the mixture was stirred for 24 hours at room temperature. After adding 500 ml of water, the solvent was distilled off under vacuum. The residue was subjected to extraction with benzene. The benzene layer was successively washed with an aqueous solution of 0.5N HCl, water, saturated sodium hydrogencarbonate and a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. The residue obtained by distilling off the solvent under vacuum was subjected to silica gel column chromatography and eluted with chloroform, whereby 9.64 g of 1α,3β-bis(triethylsilyloxy)-5-androsten-17-one was obtained as a pale yellow crystal. Part of the compound was recrystallized from methanol to give colorless needles having a melting point of 99°-100° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04891364
출처 데이터셋uspto-grants-1990_01
ORD IDord-9ea832c1589043b0a35108158ab39074
출처 메모uspto-grants-1990_01