Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288627Generated: November 2, 2026

Sodium Carbonate → [5-(4-Fluorophenyl)pyridin-3-yl]methanol

https://huagongshe.com/reaction/2288627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactant(5-Bromo-3-pyridinyl)methanolHCID 2784733—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product[5-(4-Fluorophenyl)pyridin-3-yl]methanolHCID 1554179884.4%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 3-bromo-5-hydroxymethyl-pyridine (3.3 g, 17.5 mmol) in toluene (35 ml) was added Pd(PPh3)4 (0.6 g, 0.52 mmol), an aqueous solution of Na2CO3 (17.5 ml of a 2M solution) and p-fluorphenylboronic acid (2.65 g, 19 mmol, dissolved in 8.5 ml EtOH). The mixture was heated at 80-90° C. for 1 hr and vigorously stirred. After the reaction was completed, the biphasic reaction mixture was cooled, the organic layer was collected and washed with saturated NaCl. The aqueous layer was washed with EtOAc and the combined organic layers were dried on Na2SO4. The drying agent was removed by filtration and the solvent was evaporated in vacuo to give a dark oil which was purified by flash chromatography on silica gel (eluent: CH2Cl2 /MeOH/NH4OH, 95/4.5/0.5) and yielded 3-(p-fluorophenyl)-5-hydroxymethyl-pyridine (3.0 g, 84%). The product was converted into its monohydrochloride salt; the residue was dissolved in Et2O and treated with 16.5 eq of ethanolic HCl. The product 3-(p-fluorophenyl)-5-hydroxymethyl-pyridinium hydrochloride Q4-OH.HCl precipitated as a white solid which was collected by filtration and subsequent drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090812
Source datasetuspto-grants-2000_07
ORD IDord-a0bf446ba7ac4dd3a83a08d97363ba1d
Source noteuspto-grants-2000_07