HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 12850022, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-Adamantanecarbonyl chloride | HCID 98915 | — |
| Reactant | 19-Hydroxyandrostenedione | HCID 252379 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 12850022 | HCID 12850022 | — |
Reaction Steps
A solution of 22 g of 19-hydroxyandrost-4-ene-3,17-dione, 18 g of 1-adamantanecarboxylic acid chloride, and 29 ml of pyridine in 2.2 liters of toluene is refluxed overnight. The reaction mixture is cooled, and the toluene layer is washed with water, dried over magnesium sulfate and filtered then the solvent is removed. The resulting residue is crystallized from methanol to give 19-(1-adamantanylcarbonyloxy)androst-4-ene-3,17-dione, M.P. 161°-163° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04013762 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-c9238ed8d9f4454398bd056a4afd6988 |
| Source note | uspto-grants-1977_03 |