HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → 2-(4-Benzylpiperazin-1-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(4-Benzylpiperazin-1-yl)acetonitrile | HCID 3855721 | 80% |
Reaction Steps
To a suspension of 1-benzylpiperazine (18 g) and sodium carbonate (8.3 g) in acetone (50 ml) was added chloroacetonitrile (12 g) under ice-cooling, and mixed at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure, to the residue were added water and diethyl ether, and the organic layer was collected by separation. The organic layer was washed with water and dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified with silica gel column (ethyl acetate) to obtain the title compound as pale yellow liquid (17 g, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820673B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-49746a654edc41f09f637016a9bc8aa1 |
| Source note | uspto-grants-2010_10 |