Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457741Generated: October 30, 2026

Water → HCID 22100599, compound

https://huagongshe.com/reaction/1457741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Fluorophenylboronic acidHCID 285645—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Bromo-6-fluoro-4-methylpyridineHCID 29919366—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 22100599HCID 2210059936.1%

Reaction Steps

A mixture of 2-bromo-6-fluoro-4-methylpyridine (9.5 g, 50 mmol), 4-fluorobenzeneboronic acid (7.8 g, 56 mmol), sodium bicarbonate (12.6 g, 150 mmol), water (200 mL) and catalytic amounts of tetrakis(triphenylphosphine)palladium(0) in DME under nitrogen is heated to reflux overnight. After filtration of the reaction mixture the solvents are removed under reduced pressure. The residue is partitioned between water and ethyl acetate. The layers are separated and the aqueous layer is washed with ethyl acetate. After drying of the combined organic layers with anhydrous magnesium sulphate, the solvent is removed in vacuo. The crude product is purified by flash column chromatography (silica gel, pentane/ethyl acetate 9/1) yielding colorless crystals of 2-fluoro-6-(4'-fluorophenyl)-4-methylpyridine (3.7 g, 36.1% of th.) with mp 49° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849758
Source datasetuspto-grants-1998_12
ORD IDord-689cead4b2504195a26e5c291f8efb1e
Source noteuspto-grants-1998_12