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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268704Generated: October 26, 2026

Piperidine → Ethyl 4-(3-Piperidin-1-ylpropoxy)benzoate

https://huagongshe.com/reaction/268704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantSodium CarbonateHCID 10340—
ReactantEthyl 4-(3-chloropropoxy)benzoateHCID 18348522—
CatalystPotassium IodideHCID 4875—
Solvent1-ButanolHCID 263—
SolventEthyl AcetateHCID 8857—
ProductEthyl 4-(3-Piperidin-1-ylpropoxy)benzoateHCID 17986307—

Reaction Conditions

Temperature105 °C

Reaction Steps

A stirred mixture of ethyl 4-(3-chloropropoxy)benzoate (70.0 g), piperidine (43.35 ml), sodium carbonate (45.36 g) and potassium iodide (2.37 g) in 1-butanol (650 ml) was heated at 105° C. for 16 h. The reaction was cooled to rt, diluted with EtOAc (1600 ml), washed with water (3×700 ml), saturated brine (700 ml), dried (MgSO4) and evaporated to give the title compound (D1) (82.57 g) which displayed MS and 1H NMR spectra that were identical to those of the product obtained by D1 (Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446103B2
Source datasetuspto-grants-2008_11
ORD IDord-94fe1cbe5b864289ae81f3f0848c2cf1
Source noteuspto-grants-2008_11