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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1576165생성일: 2026년 10월 25일

1,2-Dimethoxyethane → Testosterone, acetate

https://huagongshe.com/reaction/1576165

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Dibutyl methylphosphonateHCID 16994—
반응물17beta-Acetoxy-4-oxa-androst-5-en-3-oneHCID 53903713—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Testosterone, acetateHCID 92145—

반응 단계

To a suspension of 4 g. of dibutyl methylphosphonate in 75 ml. of dry monoglyme at about -78° under nitrogen, there is added with stirring one equivalent of n-butyl lithium in hexane. After about 10 minutes, there is added one equivalent of 17β-acetoxy-4-oxa-androst-5-en-3-one in 75 ml. of dry tetrahydrofuran while maintaining the temperature at about -78°. The reaction mixture is allowed to warm to room temperature and then left to stand for about four hours. The reaction mixture is diluted with water and extracted with ether. The ether extracts are combined, washed, dried and evaporated to give testosterone acetate (17β-acetoxyandrost-4-en-3-one) which can be purified by chromatography.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03979458
출처 데이터셋uspto-grants-1976_09
ORD IDord-e61a96219f5349b19110d81e6911fac4
출처 메모uspto-grants-1976_09