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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 584473생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/584473

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Benzenebutanoic acid, gamma-oxo-, methyl esterHCID 141190—
반응물Sodium AcetateHCID 517045—
반응물4-(5-Methyl-2-phenyl4-oxazolylmethoxy)benzyloxyamineHCID 22344593—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Ethyl acetate hexaneHCID 21226206—
생성물methyl (4E)-4-[[4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-4-phenylbutanoateHCID 1108140476%

반응 단계

After a mixture of 4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine (1.00 g), methyl 4-oxo-4-phenylbutyrate (619 mg), acetic acid (0.553 ml), sodium acetate (528 mg) and methanol (20 ml) was heated to reflux for 19 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-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-4-phenylbutyrate (1.18 g, yield 76%) as a colorless oil from an ethyl acetate-hexane (2:9, v/v)-eluted fraction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06924300B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-4580bc1efa6e471993dcf23b63b0543c
출처 메모uspto-grants-2005_08