HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 70477487, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 12804575 | HCID 12804575 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 70477487 | HCID 70477487 | — |
Reaction Steps
Methyl 2β-ethoxy-3α-hydroxy-11α-(3-methylbutylamino)-5α-androstane-17β-carboxylate (464 mg) in chloroform containing dry PTSA (344 mg) was stirred for 20 min, then treated with acetic anhydride (1.0 ml) and the mixture left for 3 h. The reaction mixture was diluted with ethanol and evaporated to give an oil. This was dissolved in ethyl acetate, washed with dilute ammonia solution (2×), water (1×), dried and evaporated to give an oil. This was purified by preparative t.l.c. in CHCl3 /MeOH (20:1) to give the title compound as an oil (415 mg), [α]D +27.9°, νmax 1725 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04515786 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-95734e5f188845df98d6a2255b0ac783 |
| Source note | uspto-grants-1985_05 |