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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875607Generated: October 28, 2026

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

https://huagongshe.com/reaction/875607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl nipecotateHCID 98969—
ReactantOxolane--water (1/1)HCID 21881883—
SolventDiethyl EtherHCID 3283—
ProductBenzyl ethyl piperidine-1,3-dicarboxylateHCID 1799927186.4%

Reaction Steps

To ethyl piperidine-3-carboxylate (5.0 g, 30.2 mmol) and K2CO3 (4.2 g, 30.2 mmol) in 1:1 THF-water (100 mL) was added benzyl carbonochloridate (4.5 mL, 31.7 mmol) at 0° C. The reaction mixture was stirred at room temperature for 2 hours, and then ether (50 mL) was added. The organic layer was separated, washed with brine and dried over sodium sulfate. After removal of the solvent, the residue was purified by chromatography on silica gel (hexane:ethyl acetate 5:1) to give 1-benzyl 3-ethyl piperidine-1,3-dicarboxylate (7.60 g, 86% yield) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981085B2
Source datasetuspto-grants-2015_03
ORD IDord-3d4931f5546746d9adf047d41e89edcc
Source noteuspto-grants-2015_03