HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 13131731, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 13131723 | HCID 13131723 | — |
| Product | HCID 13131731 | HCID 13131731 | — |
Reaction Steps
1.9 g of 17-benzoyloxy-11β,21-dihydroxy-6α-methyl-1,4-pregnadiene-3,20-dione is reacted, analogously to Example 2c, with acetic anhydride and worked up. The crude product is purified on 200 g of silica gel with a methylene chloride-acetone gradient (0-12% acetone), thus isolating 1.8 g of 21-acetoxy-17-benzoyloxy-11β-hydroxy-6α-methyl-1,4-pregnadiene-3,20-dione, mp 258° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04587236 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-1678e956d8254e4586940b920ddcc43c |
| Source note | uspto-grants-1986_05 |