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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 845358생성일: 2026년 10월 24일

1alpha,3beta-Diacetoxy-ergosta-5,7,22-trien → Doxercalciferol

https://huagongshe.com/reaction/845358

반응식

참여 물질

역할이름HCID투입량
반응물1alpha,3beta-Diacetoxy-ergosta-5,7,22-trienHCID 54340381—
용매Diethyl EtherHCID 3283—
생성물DoxercalciferolHCID 528110733.1%

반응 단계

1α,3β-Diacetoxy-ergosta-5,7,22-trien (X) (200 mg) from Example 7 was dissolved in ether (400 ml) and the solution was irradiated with high pressure mercury lamp (UM-452, Ushio Electric Co., Ltd.) for 10 minutes. After distilling off ether under reduced pressure, ethanol (50 ml) was added and the mixture was heated under reflux for 1 hr. Subsequently, a solution of potassium hydroxide (1 g) in ethanol (10 ml) was added and further heated under reflux for 10 minutes. The whole reaction was carried out in a nitrogen stream. After cooling, the reaction product was extracted with ether (200 ml). The extract was washed with water, dried over Na2SO4 and ether was distilled off under reduced pressure. Chromatography on silica gel of the residue (eluted with 95/5 chloroform/ethyl acetate) gave 55 mg of a crude 1α-hydroxy vitamin D2 (XI). Crystallization of the crude vitamin from hexane/acetone gave 35 mg (17.5% yield) of a pure 1α-hydroxy vitamin D2 (XI) as crystals, m.p. 146°-147° C., λ max 265 nm (ε=18500, ethanol), [α]D20 +47° (c=0.25, ethanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04758383
출처 데이터셋uspto-grants-1988_07
ORD IDord-d86e432eb9cf4cbc873ebcdcfaa4376c
출처 메모uspto-grants-1988_07