HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3alpha-Hydroxy-11-hydroxyimino-5alpha-androstane-17beta-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 3alpha-Hydroxy-5alpha-androstan-11-one 17beta-carboxylic acid | HCID 22788265 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3alpha-Hydroxy-11-hydroxyimino-5alpha-androstane-17beta-carboxylic acid | HCID 86738595 | 63.8% |
Reaction Steps
Hydroxylamine hydrochloride (4 g) was added to a water cooled solution of sodium hydroxide (50%; 16 ml). This mixture was added to a solution of 3α-hydroxy-11-oxo-5α-androstane-17β-carboxylic acid (1.5 g) in ethanol (70 ml). The mixture was heated at reflux for 24 h, cooled and brought to pH 1 with concentrated HCl solution. Water (800 ml) was added and the precipitate (1.42 g) was collected by filtration, washed with water (2×300 ml) and dried. Crystallisation from ethyl acetate gave the title compound (1 g) m.p. 250°-253° C. (dec) [α]D +124° (EtOH C=1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04353898 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-c5a1cc07a0d8496db98d4f3d483eb501 |
| Source note | uspto-grants-1982_10 |