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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584473Generated: October 25, 2026

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

https://huagongshe.com/reaction/584473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzenebutanoic acid, gamma-oxo-, methyl esterHCID 141190—
ReactantSodium AcetateHCID 517045—
Reactant4-(5-Methyl-2-phenyl4-oxazolylmethoxy)benzyloxyamineHCID 22344593—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl acetate hexaneHCID 21226206—
Productmethyl (4E)-4-[[4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-4-phenylbutanoateHCID 1108140476%

Reaction Steps

After a mixture of 4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine (1.00 g), methyl 4-oxo-4-phenylbutyrate (619 mg), acetic acid (0.553 ml), sodium acetate (528 mg) and methanol (20 ml) was heated to reflux for 19 hours, the mixture was cooled to room temperature. 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-phenyl-4-oxazolylmethoxy)benzyloxyimino]-4-phenylbutyrate (1.18 g, yield 76%) as a colorless oil from an ethyl acetate-hexane (2:9, v/v)-eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924300B2
Source datasetuspto-grants-2005_08
ORD IDord-4580bc1efa6e471993dcf23b63b0543c
Source noteuspto-grants-2005_08