HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 86737612, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 86737611 | HCID 86737611 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86737612 | HCID 86737612 | — |
Reaction Steps
A suspension of (11β,16α)-9-fluoro-11,16,17-trihydroxy-3,20-dioxopregna-1,4-dien-21-oic acid, methyl ester (150 mg) in a mixture of glacial acetic acid (5.0 ml) and acetic anhydride (5.0 ml) containing p-toluene sulfonic acid hydrate (150 mg) is stirred for 40 hours. Sodium acetate (300 mg) is added and the solution is evaporated in vacuo. The residue is diluted with water, extracted with chloroform and the chloroform extract is washed with water, dried (MgSO4) and evaporated to a solid. The solid is crystallized from ethyl acetate to afford the title compound (164 mg), melting point 317°-319° C. (dec.) (discoloration starts from ca. 280° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04257969 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-dd5435a8b671485c8ae4a61f25ec91b9 |
| Source note | uspto-grants-1981_03 |