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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095830Generated: November 1, 2026

Piperidine → 1-[3-(4-Iodophenoxy)propyl]piperidine

https://huagongshe.com/reaction/1095830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant1-(3-Chloropropoxy)-4-iodobenzeneHCID 15895520—
Product1-[3-(4-Iodophenoxy)propyl]piperidineHCID 230477372.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

1-[(3-chloropropyl)oxy]-4-iodobenzene (10 g, 33.7 mmol) and piperidine (2.87 g, 67.4 mmol) were mixed, and stirred at 85° C. for 4 hours. After cooled to room temperature, this was concentrated, and the residue was dissolved in ethyl acetate, washed with aqueous saturated sodium hydrogencarbonate solution and saturated saline, and the organic layer was dried with sodium sulfate. The solvent was evaporated off, and the residue was purified through silica gel column chromatography (eluate: ethyl acetate/hexane=50/50 to chloroform/methanol=10/1) to obtain the entitled compound (8.39 g, 72%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138206B2
Source datasetuspto-grants-2012_03
ORD IDord-caa1868cda204496aeafa1ddeaad0e28
Source noteuspto-grants-2012_03