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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15064Generated: October 26, 2026

Tetrahydrofuran → 2-Chloro-4-(4-fluorobenzyloxy)pyrimidine

https://huagongshe.com/reaction/15064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-Fluorobenzylic alcoholHCID 68022—
Reactant2,4-DichloropyrimidineHCID 77531—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
Product2-Chloro-4-(4-fluorobenzyloxy)pyrimidineHCID 8607073068%

Reaction Steps

n-Butyl lithium (2.6 M n-hexane solution, 10.1 mL) was added to tetrahydrofuran solution (12 mL) of 4-fluorobenzyl alcohol (3.08 mL) at −78° C., and stirred at the same temperature for 30 minutes. This reaction liquid was gradually added to tetrahydrofuran suspension (24 mL) of 2,4-dichloropyrimidine (4.0 g) and stirred at room temperature for 2 hours. After addition of water, the reaction liquid was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, the residue was crystallized from mixed solvent of chloroform and hexane to provide the title compound (4.36 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732456B2
Source datasetuspto-grants-2010_06
ORD IDord-ab4bf3d2c4494cc991525056ab6da85b
Source noteuspto-grants-2010_06