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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295230Generated: November 1, 2026

Water → Methyl 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolecarboxylate

https://huagongshe.com/reaction/1295230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-(Chloromethyl)-5-methyl-2-phenyl-1,3-oxazoleHCID 9794289—
ReactantHCID 178498603HCID 178498603—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolecarboxylateHCID 1786133172.4%

Reaction Steps

To a solution of methyl 3-hydroxyisoxazole-5-carboxylate (5.01 g) in N,N-dimethylformamide (70 ml) was added sodium hydride (60% in oil, 1.40 g) at 0° C. and the mixture was stirred for 15 min. Then 4-chloromethyl-5-methyl-2-phenyloxazole (7.26 g) was added and the mixture was stirred at 60° C. for 2 hrs. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and methyl 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolecarboxylate (7.96 g, yield 72%) was obtained as colorless crystals from a fraction eluted with tetrahydrofuran-hexane (1:1, volume ratio). The crystals were recrystallized from tetrahydrofuran-hexane. melting point: 123–124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241785B2
Source datasetuspto-grants-2007_07
ORD IDord-e42e971ffd8f4c3b91d94750f73c8222
Source noteuspto-grants-2007_07