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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294306Generated: November 2, 2026

Dimethylformamide → Methyl 2-[3-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolylmethoxy]phenyl]acetate

https://huagongshe.com/reaction/1294306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-HydroxyphenylacetateHCID 39129—
Reactant5-Chloromethyl-3-(5-methyl-2-phenyl-4-oxazolylmethoxy)isoxazoleHCID 17861285—
SolventWaterHCID 962—
ProductMethyl 2-[3-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolylmethoxy]phenyl]acetateHCID 6888377193%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 5-chloromethyl-3-(5-methyl-2-phenyl-4-oxazolylmethoxy)isoxazole (457 mg), methyl 2-(3-hydroxyphenyl)acetate (249 mg), anhydrous potassium carbonate (415 mg) and N,N-dimethylformamide (10 mL) was stirred at 60° C. for 3 hrs. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The obtained residue was subjected to silica gel column chromatography to give methyl 2-[3-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolylmethoxy]phenyl]acetate as a colorless oil (604 mg, 93%) from a fraction eluted with ethyl acetate-hexane (1:1, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238716B2
Source datasetuspto-grants-2007_07
ORD IDord-dea8d2f17fe54ad68238ee2b5df9c9cb
Source noteuspto-grants-2007_07