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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329591생성일: 2026년 10월 24일

Dimethoxymethane → 17beta-Acetoxy-3beta-methoxymethoxy-1alpha-methyl-17alpha-n-propyl-5alpha-androstane

https://huagongshe.com/ko/reaction/329591

반응식

참여 물질

역할이름HCID투입량
반응물DimethoxymethaneHCID 8020—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물17beta-Acetoxy-1alpha-methyl-17alpha-n-propyl-5alpha-androstan-3beta-olHCID 70360261—
용매DichloromethaneHCID 6344—
생성물17beta-Acetoxy-3beta-methoxymethoxy-1alpha-methyl-17alpha-n-propyl-5alpha-androstaneHCID 70360248—

반응 단계

400 mg of 17β-acetoxy-1α-methyl-17α-n-propyl-5α-androstan-3β-ol is combined in 2.8 ml of absolute dichloromethane and 1.8 ml of formaldehyde dimethylacetal with a mixture of 600 mg of kieselguhr W 20 and 300 mg of phosphorus pentoxide and stirred for 45 minutes at room temperature. The mixture is vacuum-filtered from the insoluble components and washed with dichloromethane containing 3-5% triethylamine. The crude product obtained after evaporation is chromatographed on silica gel, thus producing 280 mg of 17β-acetoxy-3β-methoxymethoxy-1α-methyl-17α-n-propyl-5α-androstane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04892867
출처 데이터셋uspto-grants-1990_01
ORD IDord-c964f846aaf14c5789db35504ede80cd
출처 메모uspto-grants-1990_01