HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → (6α)-17,21-Dihydroxy-6-Methylpregna-1,4,9(11)-triene-3,20-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Pregna-1,4,9(11)-triene-3,20-dione,21-(acetyloxy)-17-hydroxy-6-methyl-, (6a)- | HCID 15069866 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (6α)-17,21-Dihydroxy-6-Methylpregna-1,4,9(11)-triene-3,20-dione | HCID 15069867 | — |
Reaction Steps
A 13.58 g sample of 21-acetoxy-17α-hydroxy-6α-methylpregna-1,4,9-(11)-triene-3,20-dione in methanol (850 ml) was hydrolyzed with 10% potassium carbonate (34 ml). The reaction mixture was acidified, diluted with water and concentrated to give a gummy precipitate which was dissolved in ethyl acetate. The extract was washed with water and brine, then dried over sodium sulfate and evaporated. Crystallization of the residue from acetone-hexane gave the title compound Example 2(a), m.p. 204°-206° C.; one spot by TLC (10% CH3OH--CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04948533 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-345831ff6825430e8f5b513a5dbcc271 |
| Source note | uspto-grants-1990_08 |