HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Benzyl 4-oxopiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 4-Piperidone hydrochloride | HCID 3084851 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 4-oxopiperidine-1-carboxylate | HCID 643496 | — |
Reaction Steps
To a stirred solution of piperidin-4-one hydrochloride (1567 g, 11.56 mol) and triethylamine (1400 g, 13.87 mol) in dichloromethane (12 L) was added benzyl chloroformate (1965 g, 11.55 mol) dropwise at 0° C. After the addition, the reaction mixture was allowed to warm to room temperature and stirred overnight. TLC (EtOAc/petroleum ether=1:5) showed the reaction was complete. The mixture was washed with water (3 L) and brine (1 L), dried over sodium sulfate and concentrated to afford benzyl 4-oxopiperidine-1-carboxylate as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08183245B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-aa014a24a65e42518c3de4845d1feb09 |
| Source note | uspto-grants-2012_05 |