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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189083Generated: October 30, 2026

2-Iodopyridine → 2-(6-(4-Fluorophenyl)hexa-1,5-diynyl)pyridine

https://huagongshe.com/reaction/1189083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodopyridineHCID 221126—
Reactant1-Fluoro-4-(hexa-1,5-diynyl)benzeneHCID 86086791—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product2-(6-(4-Fluorophenyl)hexa-1,5-diynyl)pyridineHCID 1155786029.1%

Reaction Steps

In a dry reaction tube containing in suspension copper iodide (11 mg, 0.06 mmol) and triethylamine (3.4 mL), were added 2-iodopyridine (246 mg, 1.2 mmol) and Pd(PPh3)2Cl2 (42 mg, 0.06 mmol) under N2. A yellow suspension was obtained after 5 min of stirring at room temperature. A solution of 1-fluoro-4-(hexa-1,5-diynyl)benzene (210 mg, 1.2 mmol) in triethylamine (0.5 mL) was then added under N2. Immediately the color of the reaction turns to black. The mixture was stirred at room temperature for 48h. The reaction mixture was concentrated. The crude product was dissolved in DCM and the organic phase was washed with saturated NH4Cl, water and brine. The organic layer was dried over MgSO4, filtered, and concentrated. Purification by Flash chromatography (prepacked 25 g silicagel column, Cyclohexane/ethyl acetate from 90/10to 80/20 as eluent) to afford 87 mg of 2-(6-(4-fluorophenyl)hexa-1,5-diynyl)pyridine (Yield: 29%) as a brown powder (M.P.=68-69° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674106B2
Source datasetuspto-grants-2014_03
ORD IDord-53e251a90b3740718722a94dcb1453a5
Source noteuspto-grants-2014_03