HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-aminobenzoate → Ethyl 3-(piperazin-1-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-aminobenzoate | HCID 11400 | — |
| Reactant | Bis(2-chloroethyl)amine hydrochloride | HCID 522769 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Ethyl 3-(piperazin-1-yl)benzoate | HCID 11506913 | 70% |
Reaction Steps
Ethyl 3-aminobenzoate (1.65 g) was dissolved in xylene (20 ml), and bischloroethylamine hydrochloride (1.79 g) was added to the solution. The mixture was heated under reflux with stirring for two days. The solvent was removed from the reaction solution by distillation under the reduced pressure. Water and a saturated aqueous sodium hydrogencarbonate solution were added to the residue, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was then removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (chloroform:methanol=9:1-5:1) to give 1.60 g (70.0%) of ethyl 3-piperazin-1-yl-benzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06777414B1 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-a26017466ea740edb313f719fd19ce0a |
| Source note | uspto-grants-2004_08 |