HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 2-(Piperazin-1-yl)-1,3-benzoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chlorobenzoxazole | HCID 11986 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(Piperazin-1-yl)-1,3-benzoxazole | HCID 647818 | 57.1% |
Reaction Steps
In 200 ml of acetonitrile were dissolved 33.6 g (0.39 mole) of piperazine and 10.0 g (0.065 mole) of 2-chlorobenzoxazole, and 9.0 g (0.065 mole) of potassium carbonate and a catalytic amount of potassium iodide were added thereto. The mixture was refluxed by heating for 11 hours under stirring. The mixture was cooled to room temperature and then filtered. The filtrate was concentrated under reduced pressure, and the residue was applied to silica gel column chromatography (the eluent used was a mixture of chloroform : methanol = 9 : 1) to obtain 7.54 g of 1-(2-benzoxazolyl)piperazine as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05519016 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-721d03863f784a5a993efaec3c9c6757 |
| Source note | uspto-grants-1996_05 |