HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 20,20-Ethylenedioxy-5alpha-pregn-2-en-11beta-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 70583481 | HCID 70583481 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 20,20-Ethylenedioxy-5alpha-pregn-2-en-11beta-ol | HCID 70584114 | 96.8% |
Reaction Steps
20,20-Ethylenedioxy-5α-pregn-2-en-11-one (9.3 g) in hot ethanol (300 ml) was treated with sodium borohydride (5.5 g) in water (30 ml), and the mixture was refluxed on a steam bath for 1 1/2 hours, concentrated by evaporation to about 200 ml, the excess borohydride destroyed by the addition of glacial acetic acid (0.5 ml), and the mixture poured on to ice-water to give a white crystalline precipitate. The precipitate was filtered off, washed with water and dried in vacuo to give title compound (9.05 g), as colourless needles, m.p. 141°-145°, [α]D +64°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04192871 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-41912f224f024c0a94f05ba6714c788f |
| Source note | uspto-grants-1980_03 |