HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 5-[3-[4-(2-Hydroxyphenyl)-1-piperazinyl]propyl]-3-methyl-2-oxazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | o-(1-Piperazinyl)phenol dihydrobromide | HCID 3017100 | — |
| Reactant | 5-(3-Chloropropyl)-3-methyl-2-oxazolidinone | HCID 19811499 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 5-[3-[4-(2-Hydroxyphenyl)-1-piperazinyl]propyl]-3-methyl-2-oxazolidinone | HCID 19811476 | 20% |
Reaction Steps
Following the procedure of Example 5, a mixture of 1-(2-hydroxyphenyl)piperazine dihydrobromide (9.6 g, 0.0282 mol), 5-(3-chloropropyl)-3-methyl-2-oxazolidinone (5.0 g, 0.0282 mol), sodium bicarbonate (9.5 g, 0.113 mol), and potassium iodide in 1-butanol (100 ml) gave an oil. The oil was triturated several times with light pet ether (decanting each time) and dissolved in ethyl acetate/isopropyl ether. Cooling the solution gave a solid which was collected by filtration and dried under high vacuum to give 1.80 g (20% yield), mp 112°-116° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05162322 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-27186ddf7f3f4aea989e251c0c238511 |
| Source note | uspto-grants-1992_11 |