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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249587Generated: October 30, 2026

Sodium Iodide → 3-[8-[4-[2,2-Bis(3-methoxyphenyl)ethenyl]-1-piperidinyl]octyl]pyridine

https://huagongshe.com/reaction/1249587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
Reactant4-[2,2-Bis(3-methoxyphenyl)ethenyl]piperidineHCID 13754501—
Reactant3-(8-Chlorooctyl)pyridineHCID 13754505—
SolventDimethylformamideHCID 6228—
Product3-[8-[4-[2,2-Bis(3-methoxyphenyl)ethenyl]-1-piperidinyl]octyl]pyridineHCID 1375450870.1%

Reaction Steps

A mixture of 4-[2,2-bis(3-methoxyphenyl)ethenyl]piperidine (1.65 g), 3-(8-chloroctyl)pyridine (1.13 g), sodium iodide (0.75 g) and anhydrous sodium carbonate (0.53 g) in dimethylformamide (10 ml) was stirred under argon at 75° for 16 hours. The solvent was removed in vacuo and the residue was taken up in a mixture of ethyl acetate and 1N sodium hydroxide solution. The separated aqueous layer was reextracted with three portions of ethyl acetate. The organic layers were washed in turn with water and brine, then were combined, dried over sodium sulfate, decolorized with charcoal and evaporated to give 2.5 g of crude product as an oil. The oil was purified by HPLC (hexane:ethyl acetate:triethylamine; 34:17:1) to give 1.8 g of 3-[8-[4-[2,2-bis(3-methoxyphenyl)ethenyl]-1-piperidinyl]octyl]pyridine, as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04632925
Source datasetuspto-grants-1986_12
ORD IDord-da10b2eae2bf4e48bb4269013bf68395
Source noteuspto-grants-1986_12