HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethoxymethane → 17beta-Acetoxy-3beta-methoxymethyl-1alpha-methyl-17alpha-n-propyl-5alpha-androstane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethoxymethane | HCID 8020 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | 17beta-Acetoxy-1alpha-methyl-17alpha-n-propyl-5alpha-androstan-3beta-ol | HCID 70360261 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 17beta-Acetoxy-3beta-methoxymethyl-1alpha-methyl-17alpha-n-propyl-5alpha-androstane | HCID 70505065 | — |
Reaction Steps
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-methoxymethyl-1α-methyl-17α-n-propyl-5α-androstane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04456600 |
| Source dataset | uspto-grants-1984_06 |
| ORD ID | ord-46ca0d58bf674a18b94e189dd70dcef9 |
| Source note | uspto-grants-1984_06 |