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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2057생성일: 2026년 10월 23일

Tetrahydro-2-(2-propynyloxy)-2H-pyran → (8R,9S,10R,13S,14S,17S)-13-methyl-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-ol

https://huagongshe.com/ko/reaction/2057

반응식

참여 물질

역할이름HCID투입량
반응물Tetrahydro-2-(2-propynyloxy)-2H-pyranHCID 98609—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물(8R,9S,10R,13S,14S,17S)-13-methyl-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-olHCID 252818—

반응 단계

As described under 3D, 460 mg of 7G is produced from 442 mg of 7F with 1.30 ml of 2-(2-propinyloxy)tetrahydro-2H-pyrane and 5.36 ml of a 15% solution of butyllithium in hexane in 70 ml of tetrahydrofuran.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728689
출처 데이터셋uspto-grants-1998_03
ORD IDord-dda6f0d331b14af09fea8960240ce219
출처 메모uspto-grants-1998_03