HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Ethyl 4-benzyl-2-(trifluoromethyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1-Benzyl-3-(trifluoromethyl)piperazine | HCID 53407170 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-benzyl-2-(trifluoromethyl)piperazine-1-carboxylate | HCID 68748441 | — |
Reaction Steps
To a solution of 1-benzyl-3-(trifluoromethyl)piperazine 34a (1.0 mmol) and pyridine (1.1 mmol) in DCM (5 mL), is added ethyl chloroformate (1.1 mmol). The resulting mixture is stirred at rt for 1 h. After the reaction is complete, the reaction mixture is diluted with DCM (15 mL) and washed with water. The organic layer is separated, dried over Na2SO4, filtered, and concentrated to afford ethyl 4-benzyl-2-(trifluoromethyl)piperazine-1-carboxylate 34b, which is used without purification. MS (m/z) (M+1)+: 317.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08293757B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-905d12cf53f54e80aecdd4a690d6e656 |
| Source note | uspto-grants-2012_10 |