Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193675Generated: October 31, 2026

Potassium Iodide → 4-[Bis(4-fluorophenyl)methyl]-1-[3-(3,5-dimethoxyphenoxy)propyl]piperidine

https://huagongshe.com/reaction/1193675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-[Bis(4-fluorophenyl)methyl]piperidineHCID 13250544—
Reactant1-(3-Chloropropoxy)-3,5-dimethoxybenzeneHCID 14407174—
Solvent1-ButanolHCID 263—
SolventEthyl acetate hexaneHCID 21226206—
SolventEthyl acetate dimethoxyethaneHCID 87198031—
Product4-[Bis(4-fluorophenyl)methyl]-1-[3-(3,5-dimethoxyphenoxy)propyl]piperidineHCID 14407094—

Reaction Steps

A mixture of 5.51 g (0.019 mole) of 4-[bis(4-fluorophenyl)methyl]piperidine, 4.42 g (0.019 mole) of 1-(3-chloropropoxy)-3,5-dimethoxybenzene and potassium carbonate (5.53 g, 0.04 mole) was heated overnight at reflux in 350 ml of 1-butanol containing potassium iodide (0.3 g). The reaction mixture was stripped to dryness and the residue partitioned between chloroform-5% sodium hydroxide and chloroform-water. Removal of chloroform gave a brown oil. The oil was subjected to chromatography on a silica gel column using a gradient elution series of hexane-ethyl acetate and ethyl acetate-dimethoxyethane. After combining proper fractions eluted from the column and removing solvent, the residual oil was dried in vacuo overnight at 80° C. This produced 2.61 g (28.5%) of brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810713
Source datasetuspto-grants-1989_03
ORD IDord-c3ca385633b04030a9eae1086601ef75
Source noteuspto-grants-1989_03