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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875713Generated: November 3, 2026

Tetrahydrofuran → Benzyl ethyl piperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/875713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl nipecotateHCID 98969—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductBenzyl ethyl piperidine-1,3-dicarboxylateHCID 1799927186.4%

Reaction Steps

Benzyl carbonochloridate (4.5 mL, 31.7 mmol) at 0° C. was added 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). 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-e4ac9cd30c864c18a35f833ffc3b09b3
Source noteuspto-grants-2015_03