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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215517Generated: October 31, 2026

Triethylamine → 1-Benzyl 4-ethyl piperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/2215517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl 4-ethyl piperidine-1,4-dicarboxylateHCID 1528967279.5%

Reaction Steps

4-Ethoxycarbonylpiperidine (1.572 g, 10.0 mmol) was dissolved in tetrahydrofuran (50 ml); triethylamine (2.79 ml, 20.0 mmol) and benzyl chlorocarbonate (1.71 ml, 12.0 mmol) were added dropwise while cooled with an ice water bath; and the reaction mixture was stirred at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and the saturated aqueous solution of sodium hydrogencarbonate. The organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (eluent; ethyl acetate:hexane=1:3) to yield the title compound (2.315 g, 7.95 mmol, 79.5%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109219B2
Source datasetuspto-grants-2006_09
ORD IDord-37c0d978bd2f42de9a09f15da4d3734e
Source noteuspto-grants-2006_09