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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584481Generated: October 26, 2026

Dimethylformamide → methyl (4E)-4-[[4-[[5-methyl-2-(thiophen-2-ylmethyl)-1,3-oxazol-4-yl]methoxy]phenyl]methoxyimino]-4-phenylbutanoate

https://huagongshe.com/reaction/584481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Chloromethyl)-5-methyl-2-(thiophen-2-yl)-1,3-oxazoleHCID 5076491—
Reactantmethyl (4E)-4-[(4-hydroxyphenyl)methoxyimino]-4-phenylbutanoateHCID 10946929—
ReactantEthyl acetate hexaneHCID 21226206—
SolventWaterHCID 962—
Productmethyl (4E)-4-[[4-[[5-methyl-2-(thiophen-2-ylmethyl)-1,3-oxazol-4-yl]methoxy]phenyl]methoxyimino]-4-phenylbutanoateHCID 2234462363%

Reaction Steps

A mixture of 4-(chloromethyl)-5-methyl-2-(2-thienyl)oxazole (376 mg), methyl E-4-[(4-hydroxybenzyloxy)imino]-4-phenylbutyrate (500 mg), potassium carbonate (442 mg) and N,N-dimethylformamide (10 ml) was stirred at room temperature for 40 hours. Water was added to the reaction mixture and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was subjected to silica gel chromatography to obtain methyl E-4-[4-[5-methyl-2-(2-thenyl)-4-oxazolylmethoxy]benzyloxyimino]-4-phenylbutyrate (495 mg, yield 63%) as a colorless oil from an ethyl acetate-hexane (1:5, v/v)-eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924300B2
Source datasetuspto-grants-2005_08
ORD IDord-a9663b748db64264811de2b0c6e62dbe
Source noteuspto-grants-2005_08