HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxazolidin → HCID 20391701, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxazolidin | HCID 4641 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 20391701 | HCID 20391701 | — |
Reaction Steps
First, 1-Phenyl-2-(4'-acetyloxyphenyl)-3,5-pyrazolidinedione was prepared as follows. Oxyphenbutazone (1.00 g, 3.1 mmole) was suspended in 4 ml of glacial acetic acid and allowed to react with 2 ml of acetyl chloride at room temperature overnight. The solution was concentrated in vacuo at 86° C. to give a white residue (mp 126°-130° C.). The residue was crystallized from chloroformheptane (6:50) with cooling to give 0.81 g (mp 132°-134° C., 71% yield, lit., R. Pfester and F. Hafliger, Helvetica Chemica Acta, 40, 395 (1957) mp 135°-137° C. from methanol) of 1-phenyl-2-(4'-acetyloxyphenyl)-3,5-pyrazolidinedione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04117232 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-e46c195e8e4d4def804360890729e9ec |
| Source note | uspto-grants-1978_09 |