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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659948Generated: October 27, 2026

4-Fluorobenzyl chloride → 4-[2-(4-Fluoro-phenyl)-1,1-dimethoxy-ethyl]-pyridine

https://huagongshe.com/reaction/659948

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzyl chlorideHCID 9602—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(Dimethoxymethyl)pyridineHCID 642853—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-[2-(4-Fluoro-phenyl)-1,1-dimethoxy-ethyl]-pyridineHCID 1495622694.8%

Reaction Steps

315 mL of n-butyllithium 1.6 M solution in hexane is added dropwise to a solution of 70.3 g (0.46 mole) of 4-dimethoxymethyl-pyridine in 1.4 L of tetrahydrofuran under nitrogen at −70° C. After 30 min. at −70° C., 73 g (0.505 mole) of 4-fluorobenzyl chloride in 280 mL of tetrahydrofuran is added dropwise. After 10 more min. at −70° C., the reaction mixture is allowed to reach room temperature and then stirred for 30 further min. The reaction mixture is poured into 2 L ammonium chloride solution and extracted with ethyl acetate. The organic phase is washed with water and dried over magnesium sulfate. After concentration the residue is purified by chromatography on silica gel (ethylacetate/hexane 1/1) to give 114 g of 4-[2-(4-Fluoro-phenyl)-1,1-dimethoxy-ethyl]-pyridine as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084395B2
Source datasetuspto-grants-2011_12
ORD IDord-5c983e7399a649d69d87e3adb06b90bd
Source noteuspto-grants-2011_12