HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 19-Hydroxy-1beta-methyl-5-androstene-3,17-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 19-Hydroxy-1beta-methyl-4-androsten-3,17-dione | HCID 54279369 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 19-Hydroxy-1beta-methyl-5-androstene-3,17-dione | HCID 70606520 | — |
Reaction Steps
To a solution of potassium t-butoxide in dimethylsulfoxide at 25° C. under nitrogen is added with stirring 19-hydroxy-1β-methyl-4-androstene-3,17-dione in dimethylsulfoxide. After 15 minutes the mixture is poured onto a cold aqueous ammonium chloride solution. The solid is rapidly filtered, washed well with water and dissolved in ether. The ether solution is again washed with water and dried over sodium sulfate. The ether is removed at room temperature to yield 19-hydroxy-1β-methyl-5-androstene-3,17-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04139617 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-3eabafddfbe5472496586451cd8416ff |
| Source note | uspto-grants-1979_02 |