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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923651Generated: November 2, 2026

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

https://huagongshe.com/reaction/1923651

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 numberUS08178131B2
Source datasetuspto-grants-2012_05
ORD IDord-0bfe9654f5324333b98ff9d8b9affe00
Source noteuspto-grants-2012_05