HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dipotassium 2,3-dihydroxybutanedioate → 19-Tetrahydropyranyloxy-1,5-androstadiene-3beta,17beta-diol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dipotassium 2,3-dihydroxybutanedioate | HCID 6100505 | — |
| Reactant | Lithium tri-tert-butoxyaluminohydride | HCID 16710494 | — |
| Reactant | 19-Tetrahydropyranyloxy-1,5-androstadiene-3,17-dione | HCID 22806902 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 19-Tetrahydropyranyloxy-1,5-androstadiene-3beta,17beta-diol | HCID 22806903 | — |
Reaction Steps
A tetrahydrofuran solution of 19-tetrahydropyranyloxy-1,5-androstadiene-3,17-dione is added under nitrogen to a solution of lithium tri-t-butoxyaluminum hydride in tetrahydrofuran. After stirring overnight at room temperature, an aqueous solution of potassium tartrate is added with stirring to form a readily filterable white solid. The reaction mixture is filtered, the filtrate dried over magnesium sulfate and the solvent removed by evaporation. The residue which remains is crystallized from an acetone solution to yield 19-tetrahydropyranyloxy-1,5-androstadiene-3β,17β-diol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04139617 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-ae27a436963a44bd931b8437c65ace27 |
| Source note | uspto-grants-1979_02 |