HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 70477852, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Reactant | HCID 12804606 | HCID 12804606 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 70477852 | HCID 70477852 | — |
Reaction Steps
Methyl 11α-cyclohexylamino-3α-hydroxy-5α-androstane-17β-carboxylate (740 mg) in chloroform (8 ml) containing dry PTSA (640 mg) was stirred for 20 min then treated with acetic anhyride (1.9 ml) and left for 20 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×) and water (1×), dried and evaporated to give a foam. This was purified by preparative t.l.c. in chloroform/methanol (9:1) to give a foam which was crystallised from acetonitrile to give the title compound, m.p. 87°-89° [α]D +16.9°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04515786 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-755fcf2e9eb34dda9817568692988675 |
| Source note | uspto-grants-1985_05 |