HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 5-[2-[4-(3-Fluorophenyl)-1-Piperazinyl]Ethyl]-3-Methyl-2-Oxazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(3-Fluorophenyl)piperazine | HCID 77418 | — |
| Reactant | 5-(2-Chloro-ethyl)-3-methyl-oxazolidin-2-one | HCID 14698746 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 5-[2-[4-(3-Fluorophenyl)-1-Piperazinyl]Ethyl]-3-Methyl-2-Oxazolidinone | HCID 15030069 | — |
Reaction Steps
A mixture of 8.0 g (0.044 mol) of 1-(3-fluorophenyl)piperazine, 8.0 g (0.049 mol) of 5-(2-chloroethyl)-3-methyl-2-oxazolidinone, 18.7 g (0.176 mol) of anhydrous sodium carbonate, and 0.3 g (0.002 mol) of potassium iodide in 250 mL of 1-butanol was heated at reflux for 16 h. The mixture was concentrated under reduced pressure and the residue partitioned between 300 mL of benzene and 300 mL of water. The benzene layer was washed with water and brine, dried (MgSO4) and concentrated under reduced pressure to give a light-yellow solid. The solid was recrystallized from benzene-petroleum ether (30°-60° C.) to yield 9.5 g (70%) of white soldi, mp 92°-93° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05086055 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-9cf1690d38934372a5121430742727c9 |
| Source note | uspto-grants-1992_02 |