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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780067Generated: October 26, 2026

Ethanol → 3-Chloro-2,5-di(4-octyloxyphenyl)pyridine

https://huagongshe.com/reaction/1780067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant4-n-Octyloxyphenylboronic Acid (contains varying amounts of Anhydride)HCID 3977284—
Reactant5-Bromo-3-chloro-2-(4-octyloxyphenyl)pyridineHCID 19050004—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3-Chloro-2,5-di(4-octyloxyphenyl)pyridineHCID 1904999348.9%

Reaction Steps

2.00 g (5.40 mmol) of 5-bromo-3-chloro-2-(4-octyloxyphenyl)pyridine, 1.50 g (6.00 mmol) of 4-octyloxybenzeneboronic acid, 0.07 g (0.6 mmol) of tetrakis(triphenylphosphine)palladium(0) and 1.3 g (12.00 mmol) of sodium carbonate are heated at 80° C. for 3 hours in 20 ml of toluene, 10 ml of ethanol and 10 ml of water. The mixture is subsequently partitioned between aqueous sodium chloride solution and ether, the organic phase is washed with aqueous sodium chloride solution, dried over sodium sulfate and evaporated, and the product is purified by chromatography (silica gel/dichloromethane), giving 1.38 g of 3-chloro-2,5-di(4-octyloxyphenyl)pyridine. ##STR24##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629428
Source datasetuspto-grants-1997_05
ORD IDord-6369c675c53c486b9e2852c43191dc58
Source noteuspto-grants-1997_05