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HRID 1070157作成日:2026年10月27日

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

https://huagongshe.com/reaction/1070157

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物3-(Chloromethyl)-5-phenyl-1,2-oxazoleHCID 1484769—
反応物Ethyl acetate hexaneHCID 21226206—
反応物4-Hydroxybenzyloxyimino-4-phenylbutyrateHCID 131722723—
溶媒WaterHCID 962—
生成物methyl (4E)-4-phenyl-4-[[4-[(5-phenyl-1,2-oxazol-3-yl)methoxy]phenyl]methoxyimino]butanoateHCID 1173037863%

反応手順

A mixture of 3-(chloromethyl)-5-phenylisoxazole (340 mg), methyl E-4-(4-hydroxybenzyloxyimino-4-phenylbutyrate (500 mg), potassium carbonate (442 mg) and N,N-dimethylformamide (10 ml) was stirred at room temperature for 72 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-phenyl-4-[4-(5-phenyl-3-isoxazolylmethoxy)benzyloxyimino]butyrate (472 mg, yield 63%) as a colorless oil from an ethyl acetate-hexane (2:9, v/v)-eluted fraction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06251926B1
出典データセットuspto-grants-2001_06
ORD IDord-32b3656aa86744a79e99edc5c2c75771
出典メモuspto-grants-2001_06