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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 584453생성일: 2026년 10월 26일

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/584453

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1H-Indene-1-carboxylic acid, 2,3-dihydro-3-oxo-HCID 99815—
반응물Sodium AcetateHCID 517045—
반응물4-(5-Methyl-2-phenyl4-oxazolylmethoxy)benzyloxyamineHCID 22344593—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물(3E)-3-[[4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-1,2-dihydroindene-1-carboxylic acidHCID 1099429269.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06924300B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-30ec2f7c7b0f42bbbb15b5d332add124
출처 메모uspto-grants-2005_08