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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923753Generated: November 4, 2026

Tetrahydrofuran → Benzyl ethyl piperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/1923753

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 numberUS08178131B2
Source datasetuspto-grants-2012_05
ORD IDord-185d1d24aa104c3c9befb16c2f21ede2
Source noteuspto-grants-2012_05