HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl chloroformate → Benzyl ethyl piperidine-1,3-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Ethyl nipecotate | HCID 98969 | — |
| Reactant | Ethyl 1-benzoyl-3-piperidinecarboxylate | HCID 3784394 | — |
| Product | Benzyl ethyl piperidine-1,3-dicarboxylate | HCID 17999271 | — |
Reaction Steps
The reaction was run in the same manner as ethyl 1-benzoyl-3-piperidinecarboxylate, starting with ethyl nipecotate (209.9 mg; 1.33 mmol and benzyl chloroformate (190 μl; 1.33 mmol). The crude product was distilled at 220° C./0.1 torr, giving ethyl 1-benzyloxycarbonyl-3-piperidinecarboxylate (236.5 mg) as a colorless oil. MS m/Z (positive ion) 539 ([dimer-OEt]+; 50), 337 (M+2Na+; 25), 314 (M+Na+; 50), 292 (MH+; 100), 247.5 (M-OEt; 90), 158 (50).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06664271B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-05481e83f1b34492a5c9a7a84d1586d0 |
| Source note | uspto-grants-2003_12 |