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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 551839생성일: 2026년 10월 25일

3,4-dihydro-2H-pyran → 3beta-(2-Tetrahydropyranoxy)androst-5-ene-7,17-dione

https://huagongshe.com/reaction/551839

반응식

참여 물질

역할이름HCID투입량
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물7-Keto-dehydroepiandrosteroneHCID 193313—
반응물Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
생성물3beta-(2-Tetrahydropyranoxy)androst-5-ene-7,17-dioneHCID 69736313—

반응 단계

3β-hydroxyandrost-5-ene-7,17-dione (2) (0.5 g, 1.65 mmol) was placed in a dried, argon-flushed flask where it was dissolved in dry dichloromethane (20.0 mL). Pyridinium toluene-p-sulfonate (0.043 g. 0.17 mmol) was added followed by 3,4-dihydro-2H-pyran (0.23 mL, 2.5 mmol) and the solution was stirred at room temperature, under an atmosphere of argon, for 2-3 h. The reaction was quenched by adding water and the product was extracted thrice with ether (3×20 mL). The combined ether extracts were washed with dilute acetic acid, water and bicarbonate solution and dried (MgSO4). Solvent was removed and the crude product was purified using chromatography on silica gel (ethyl acetate-hexane, 15:85, v/v). The compound first eluted was identified as androsta-3,5-diene-7,17-dione (0.150 g), m.p. 167-8° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947846B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-963224c3229448e38d54c7f58113781d
출처 메모uspto-grants-2011_05