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HRID 584464Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/584464

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktBenzenebutanoic acid, gamma-oxo-, methyl esterHCID 141190—
EduktSodium AcetateHCID 517045—
Edukt3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamineHCID 10924946—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produktmethyl (4E)-4-[[3-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-4-phenylbutanoateHCID 1176262861%

Reaktionsschritte

After a mixture of 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine (600 mg), methyl 4-oxo-4-phenylbutyrate (371 mg), acetic acid (0.331 ml), sodium acetate (317 mg) and methanol (20 ml) was heated to reflux for 40 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-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-4-phenylbutyrate (570 mg, yield 61%) as a colorless oil from an ethyl acetate-hexane (1:4, v/v)-eluted fraction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06924300B2
Quelldatensatzuspto-grants-2005_08
ORD IDord-9355021df79947bb854939804521962e
Quellennotizuspto-grants-2005_08