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HRID 1070135作成日:2026年10月27日

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

https://huagongshe.com/reaction/1070135

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1H-Indene-1-carboxylic acid, 2,3-dihydro-3-oxo-HCID 99815—
反応物Sodium AcetateHCID 517045—
反応物4-(5-Methyl-2-phenyl4-oxazolylmethoxy)benzyloxyamineHCID 22344593—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物(3E)-3-[[4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-1,2-dihydroindene-1-carboxylic acidHCID 1099429269.2%

反応手順

After a mixture of 4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine (500 mg), 3-oxo-1-indancarboxylic acid (284 mg), acetic acid (0.276 ml), sodium acetate (264 mg) and ethanol (20 ml) was heated to reflux for 18 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 recrystallized from ethyl acetate-hexane to obtain E-3-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-1-indancarboxylic acid (522 mg, yield 69%) as colorless crystals. m.p. 148-149° C.

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-40ae20dc8a2b470287de4ef389a37805
出典メモuspto-grants-2001_06