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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349950Generated: October 25, 2026

Dimethylformamide → Methyl 5-(5-methyl-2-phenyl-4-oxazolyl)methoxy-3-pyridinecarboxylate

https://huagongshe.com/reaction/349950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-hydroxypyridine-3-carboxylateHCID 354317—
Reactant4-(Chloromethyl)-5-methyl-2-phenyl-1,3-oxazoleHCID 9794289—
SolventWaterHCID 962—
ProductMethyl 5-(5-methyl-2-phenyl-4-oxazolyl)methoxy-3-pyridinecarboxylateHCID 1786134159.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of methyl 5-hydroxy-3-pyridinecarboxylate (9.84 g), 4-chloromethyl-5-methyl-2-phenyloxazole (13.40 g), potassium carbonate (8.90 g) and N,N-dimethylformamide (100 ml) was stirred at 80° C. overnight. The reaction mixture was poured into water, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and concentrated. The residue was subjected to silica gel column chromatography to obtain methyl 5-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridinecarboxylate (12.42 g, yield 59%) as pale yellow crystals from the fraction eluted with ethyl acetate-hexane (1:2, volume ratio). This was recrystallized from ethyl acetate-hexane. Melting point: 119–120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-4b6f402531fb40e68251360b27c030a2
Source noteuspto-grants-2007_02