HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 5-[2-[4-(4-Bromophenyl)-1-piperazinyl]ethyl]-3-methyl-2-oxazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(4-Bromophenyl)piperazine | HCID 2735629 | — |
| Reactant | 5-(2-Chloro-ethyl)-3-methyl-oxazolidin-2-one | HCID 14698746 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 5-[2-[4-(4-Bromophenyl)-1-piperazinyl]ethyl]-3-methyl-2-oxazolidinone | HCID 15030074 | 76% |
Reaction Steps
This compound was prepared according to the procedure of Example 2. A mixture of 3.6 g (0.015 mol) of 1-(4-bromophenyl)piperazine, 2.5 g (0.015 mol) of 5-(2-chloroethyl)-3-methyl-2-oxazolidinone, 4.8 g (0.045 mol) of anhydrous sodium carbonate and 0.4 g of potassium iodide in 100 mL of 1-butanol heated at reflux for 22 h gave 4.2 g (76%) of white solid, mp 125°-127° C. (2-propanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05086055 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-94689c0621fb48f7927b7346d20edde4 |
| Source note | uspto-grants-1992_02 |