HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 19-Tetrahydropyranyloxy-1,5-androstadiene-3,17-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 19-Tetrahydropyranyloxy-1,4-androstadiene-3,17-dione | HCID 22806901 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 19-Tetrahydropyranyloxy-1,5-androstadiene-3,17-dione | HCID 22806902 | — |
Reaction Steps
To a solution of potassium t-butoxide in dimethylsulfoxide at 25° C. under nitrogen is added 19-tetrahydropyranyloxy-1,4-androstadiene-3,17-dione in dimethylsulfoxide with stirring. After 15 minutes the mixture is poured onto cold aqueous solution of ammonium chloride. The solid which forms is rapidly filtered, washed well with water and dissolved in ether. The ether solution is washed with water, dried over sodium sulfate and evaporated at room temperature to yield 19-tetrahydropyranyloxy-1,5-androstadiene-3,17-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04139617 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-0e0e7384f68941c4b02dda1f7564c6c4 |
| Source note | uspto-grants-1979_02 |