Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dimethoxymethane → 17beta-Acetoxy-3beta-methoxymethoxy-1alpha-methyl-17alpha-n-propyl-5alpha-androstane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dimethoxymethane | HCID 8020 | — |
| 반응물 | Phosphorus oxide (P4O10) | HCID 14812 | — |
| 반응물 | 17beta-Acetoxy-1alpha-methyl-17alpha-n-propyl-5alpha-androstan-3beta-ol | HCID 70360261 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 17beta-Acetoxy-3beta-methoxymethoxy-1alpha-methyl-17alpha-n-propyl-5alpha-androstane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04892867 |
| 출처 데이터셋 | uspto-grants-1990_01 |
| ORD ID | ord-c964f846aaf14c5789db35504ede80cd |
| 출처 메모 | uspto-grants-1990_01 |