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HRID 584464作成日:2026年10月26日

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

https://huagongshe.com/reaction/584464

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Benzenebutanoic acid, gamma-oxo-, methyl esterHCID 141190—
反応物Sodium AcetateHCID 517045—
反応物3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamineHCID 10924946—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物methyl (4E)-4-[[3-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-4-phenylbutanoateHCID 1176262861%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06924300B2
出典データセットuspto-grants-2005_08
ORD IDord-9355021df79947bb854939804521962e
出典メモuspto-grants-2005_08