HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → H3ST8XN423
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 9beta,11beta-Epoxy-17,21-dihydroxypregna-1,4-diene-3,20-dione 21-acetate | HCID 11876290 | — |
| Reactant | Isopropenylacetate | HCID 18355900 | — |
| Product | H3ST8XN423 | HCID 86737547 | — |
Reaction Steps
10 g of sulfonic acid resin (Amberlite I R120, marketed by Rohm and Haas Co.) was dehydrated by azeotropic destillation with benzene. The dry resin was suspended in 50 ml isopropenylacetate and 10 g 9β,11β-epoxy-21-acetoxy-17-hydroxy-pregna-1,4-diene-3,20-dione were added. The mixture was heated under reflux for 5 hours, cooled and filtered an the filtrate was evaporated to dryness. The residue which crystallized from methanol (0,5% pyridine) gave in high yield (9,5 grams) 3,21-diacetoxy-17-hydroxy-9β,11β-epoxy-pregna-1,3,5-triene-20-one. Melting point: 194° C., λmax 310 nm (ε5500)⟦alpha⟧sub.D in chloroform -199° C. (c=1% chloroform), νmax (cm-1) (K Br) 3450; 1765; 1740; 1725; 1655; 1625; 1590.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04255331 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-4fa835e709e2426385a04f0a6c8137c7 |
| Source note | uspto-grants-1981_03 |