HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 3-Methyl-5-(4-Phenyl-1-Piperazinylmethyl)-2-Oxazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-(Chloromethyl)-3-methyl-2-oxazolidinone | HCID 12889925 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 3-Methyl-5-(4-Phenyl-1-Piperazinylmethyl)-2-Oxazolidinone | HCID 15030097 | 16.3% |
Reaction Steps
This compound was prepared according to the procedure of Example 2. A mixture of 3.2 g (0.02 mol) of 1-phenylpiperazine, 3.0 g (0.02 mol) of 5-(chloromethyl)-3-methyl-2-oxazolidinone, 8.0 g (0.075 mol) of anhydrous sodium carbonate, and 0.4 g of potassium iodide in 100 mL of 1-butanol gave a brown oil as residue. The oil was converted to the dioxalate and the solid was recrystallized from acetonitrile-dimethylformamide but did not give a correct combustion analysis. The salt was partitioned between methylene chloride and a 4% sodium hydroxide solution. The organic layer was dried (Na2SO4) and concentrated to yield 0.9 g (16%) of white solid, mp 110°-112° C. (2-propanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05086055 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-2ad6af93b3db4b0e8d0bbbbabe3db175 |
| Source note | uspto-grants-1992_02 |