HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → WS-5995 A
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 178490201 | HCID 178490201 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | WS-5995 A | HCID 156387 | — |
Reaction Steps
The entire amount of the 2-(3,5-dihydroxy-1,4-naphthoquinon-2-yl)-3-methoxy-5-methylbenzoic acid obtained above was dissolved in ethyl acetate (10 ml) and while the solution was stirred at room temperature, a mixture (1 ml:10 ml) of trifluoroacetic anhydride and acetic anhydride was added. The mixture was further stirred at the same temperature for an hour. This reaction mixture was washed with water and dilute aqueous sodium carbonate in that order, followed by drying over magnesium sulfate. The solvent was then distilled off and the residual brown oil was subjected to silica gel column chromatography to give vermillion-colored crystals (20 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04414226 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-49de84f189fc489eb8cd3c29f3853600 |
| Source note | uspto-grants-1983_11 |