HuagongsheHuagongshe Chemistry Print Report · For research reference only
18000-76-5 → HCID 70601729, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 18000-76-5 | HCID 10830433 | — |
| Reactant | HCID 10903773 | HCID 10903773 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70601729 | HCID 70601729 | — |
Reaction Steps
1.1 g. of 3β-methoxymethoxy-5-androsten-17-one is hydrogenated as disclosed in Example 25. The thus-obtained crude product is not quite uniform and contains, in addition to 3β-methoxymethoxy-5α-androstan-17-one, of which 0.65 g. can be obtained by crystallization from methanol, also proportions of 3β-methoxymethoxy-5α-androstan-17β-ol. By continuing the hydrogenation or by reduction with sodium borohydride, this product becomes the primary yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04179336 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-4721e52898924a49b3aed794cfc1aef4 |
| Source note | uspto-grants-1979_12 |