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HRID 1070146作成日:2026年10月25日

Acetic Acid → ethyl (2E)-2-[[3-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-6-phenylhexanoate

https://huagongshe.com/reaction/1070146

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Sodium AcetateHCID 517045—
反応物Ethyl 6-oxo-6-phenylhexanoateHCID 3681727—
反応物3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamineHCID 10924946—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物ethyl (2E)-2-[[3-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-6-phenylhexanoateHCID 8820225858.1%

反応手順

After a mixture of 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine (600 mg), ethyl 6-oxo-6-phenylhexanoate (452 mg), acetic acid (0.331 ml), sodium acetate (317 mg) and ethanol (20 ml) was heated to reflux for 15 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 ethyl E-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-6-phenylhexanoate (590 mg, yield 58%) 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-416bd9e55a0942f8a01316bbeec1cc80
出典メモuspto-grants-2001_06