HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzylpiperazine → 7-Methoxy-4-{[4-benzylpiperazinyl]methyl}chromen-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | 4-Bromomethyl-7-methoxycoumarin | HCID 121894 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Methoxy-4-{[4-benzylpiperazinyl]methyl}chromen-2-one | HCID 1106748 | — |
Reaction Steps
0.03 mol of 1-benzylpiperazine, 0.03 mol of 7-methoxy-2-oxo-4-bromomethyl-3-chromene and 0.03 mol of potassium bicarbonate are introduced into an Erlenmeyer flask containing 150 ml of tetrahydrofuran. The mixture is brought to reflux for 24 hours. The reaction is brought to an end and, after cooling, the solution is filtered and evaporated under reduced pressure. The residue is then purified by chromatography on a column of silica gel, methylene chloride generally being used as eluent. The final product is thus obtained in the base form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05668138 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-5b36025d051f46c293507735243774b2 |
| Source note | uspto-grants-1997_09 |