HuagongsheHuagongshe Chemistry Print Report · For research reference only
2beta-Ethyl-17beta-methoxy-5alpha-androstan-3-one → 2alpha-Ethyl-17beta-methoxy-5alpha-androstan-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2beta-Ethyl-17beta-methoxy-5alpha-androstan-3-one | HCID 70562822 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2alpha-Ethyl-17beta-methoxy-5alpha-androstan-3-one | HCID 12836849 | — |
Reaction Steps
2β-Ethyl-17β-methoxy-5α-androstan-3-one (Step A) is dissolved in ethanol (95%, 13 ml.) followed by addition of sodium hydroxide (50%, 14 drops). After stirring at 20°-25° for 4.5 hrs. the mixture is extracted with diethyl ether, the diethyl ether extract is concentrated under reduced pressure to yield the title compound, which is recrystallized twice from methanol; m.p. 105°-107°; NMR (CDCl3) 0.77, 1.05, 3.20 and 3.33 δ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04297350 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-3363d3422175400f96ff40f04c7fae26 |
| Source note | uspto-grants-1981_10 |