HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 16657482, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thioacetic acid | HCID 10484 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,20-Dioxopregna-4,6-dien-21-yl acetate | HCID 3080724 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 16657482 | HCID 16657482 | — |
Reaction Steps
The product of Example 3 was hydrolyzed by treating 0.5 g of the 21-acetoxy derivative in 8 ml methylene chloride with 10 ml methanol and 4 ml 0.2M aqueous potassium carbonate at room temperature under nitrogen for 30 minutes. The hydrolyzed product was extracted with methylene chloride, washed with water, dried and evaporated. A sample obtained by preparative high performance liquid chromatography showed M+ =404 daltons. An identical product was obtained by a different synthetic route involving alkaline hydrolysis of 21-acetoxy-4,6-pregnadiene-3,20-dione to the C-21-alcohol, followed by reaction with ethanethiolic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04603128 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-680aeeb5c20f494cbe5d0e2bf869ed3a |
| Source note | uspto-grants-1986_07 |