HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → Tert-butyl 4-(cyanomethyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Tert-butyl 4-(cyanomethyl)piperazine-1-carboxylate | HCID 21936030 | — |
Reaction Steps
To a stirred solution of N-Boc piperazine (1 g) in dry THF (20 ml), triethylamine (3 ml), followed by chloroacetonitrile (5.02 ml) were added dropwise. The reaction mixture was allowed to stir at room temperature for overnight. The solvent was removed under vacuum and residue was diluted ethyl acetate (20 ml). The organic layer was concentrated to dryness under reduced pressure to afford tert-butyl 4-(cyanomethyl)piperazine-1-carboxylate, which was used for the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807671B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-7f645550e2b74a4886aa6b6fc1f29716 |
| Source note | uspto-grants-2010_10 |