HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 13092028, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 13092027 | HCID 13092027 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 13092028 | HCID 13092028 | — |
Reaction Steps
5-(2-Aminophenyl)oxazolidine-2,4-dione hydrochloride (1 g., 4.37 mmoles) were taken into 15 ml. of glacial acetic acid. Sodium acetate (358 mg., 4.37 mmoles) were added and then, in a dropwise manner, acetic anhydride (449 mg., 0.41 ml., 4.37 mmoles). The reaction mixture was stirred at room temperature for 16 hours, poured into 50 ml. of water and extracted with three portions of ethyl acetate. The combined extracts were washed with two portions of water and then one of brine, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo solids (0.72 g.). Recrystallization from ethyl acetate gave purified 5-(2-acetamidophenyl)oazolidine-2,4-dione in two crops (0.26 g., m.p. 197°-198° C.; m/e 234].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04367234 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-281248d301214d89b688f9b599216a19 |
| Source note | uspto-grants-1983_01 |