Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432791Generated: October 30, 2026

Benzyl chloroformate → Benzyl ethyl piperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/432791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantEthyl nipecotateHCID 98969—
ReactantEthyl 1-benzoyl-3-piperidinecarboxylateHCID 3784394—
ProductBenzyl ethyl piperidine-1,3-dicarboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664271B1
Source datasetuspto-grants-2003_12
ORD IDord-05481e83f1b34492a5c9a7a84d1586d0
Source noteuspto-grants-2003_12