HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 4-[4-(4-Tert-butyl-phenyl)-piperazin-1-yl]-butyric acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | 1-(4-tert-Butylphenyl)piperazine | HCID 781722 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[4-(4-Tert-butyl-phenyl)-piperazin-1-yl]-butyric acid ethyl ester | HCID 58576458 | 84.8% |
Reaction Steps
A mixture of 1-(4-tert-butyl-phenyl)-piperazine (1.09 mg; 5.0 mmol), 4-bromo-butyric acid ethyl ester (975 mg; 5.0 mmol), potassium carbonate (691 mg; 5.0 mmol) and potassium iodide (914 mg; 5.5 mmol) in acetonitrile (15 mL) is heated to reflux for 2 hours. The reaction mixture is allowed to attain room temperature and all solids removed by filtration. The filtration residue is washed with acetonitrile and the filtrate concentrated under high vacuum to afford the desired compound (1.41 g; 4.24 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096524B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-6e19fe14b5e54f6290f575841c691bff |
| Source note | uspto-grants-2015_08 |