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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432796Generated: October 25, 2026

Benzyl chloroformate → 1-Benzyl 3-ethyl 4-oxopiperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/432796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Piperidinecarboxylic acid, 4-oxo-, ethyl ester, hydrochloride (1:1)HCID 107315—
ReactantEthyl 1-benzoyl-3-piperidinecarboxylateHCID 3784394—
Product1-Benzyl 3-ethyl 4-oxopiperidine-1,3-dicarboxylateHCID 4460776362%

Reaction Steps

The reaction was run in the same manner as ethyl 1-benzoyl-3-piperidinecarboxylate, starting with commercially available ethyl 4-piperidone-3-carboxylate hydrochloride (203.2 mg; 0.98 mmol), diisopropylethylamine (360 μl; 2.08 mmol), and benzyl chloroformate (141 μl; 0.99 mmol). The crude product was purified by chromatography on silica eluting with 15% ethyl acetate in hexane, giving ethyl 1-benzyloxycarbonyl-4-oxo-3-piperidinecarboxylate (185.5 mg) as a colorless oil. MS m/z (positive ion) 323 (M+NH4+; 75), 306 (MH+; 100), 262 (50).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664271B1
Source datasetuspto-grants-2003_12
ORD IDord-d3c5f8ef66c34329a022e0ed258d0d37
Source noteuspto-grants-2003_12