HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethanol → 1-(2-Hydroxyethyl)-1-methyl-4-(benzoxazol-2-yl)homo-piperazinium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethanol | HCID 12225 | — |
| Reactant | 2-(4-Methyl-1-homopiperazinyl)benzoxazole | HCID 10585621 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Hydroxyethyl)-1-methyl-4-(benzoxazol-2-yl)homo-piperazinium iodide | HCID 19047276 | — |
Reaction Steps
A 100 mg portion of 2-(4-methyl-1-homopiperazinyl)-benzoxazole was dissolved in 3 ml of THF. Under cooling with ice, 89 mg of 2-iodoethyl alcohol was added to the thus prepared solution, and the reaction was carried out for 1 hour at the same temperature and then for 29 hours at room temperature. The reaction solution was concentrated under a reduced pressure, and 3 ml of acetone was added to the resulting residue. The precipitate thus formed was collected by filtration, washed with acetone and then dried to obtain 143 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05631257 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-3c1c44bac39e4726bd010ab1cffe6729 |
| Source note | uspto-grants-1997_05 |