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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 584454생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/584454

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium AcetateHCID 517045—
반응물Ethyl 4-oxo-4-(2-pyridyl)butyrateHCID 10104463—
반응물4-(5-Methyl-2-phenyl4-oxazolylmethoxy)benzyloxyamineHCID 22344593—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Ethyl acetate hexaneHCID 21226206—
생성물ethyl (4E)-4-[[4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-4-pyridin-2-ylbutanoateHCID 1107112175%

반응 단계

After a mixture of 4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine (500 mg), ethyl 4-oxo-4-(2-pyridyl)butyrate (367 mg), acetic acid (0.276 ml), sodium acetate (264 mg) and ethanol (20 ml) was heated to reflux for 20 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-4-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-4-(2-pyridyl)butyrate (600 mg, yield 75%) as a colorless oil from an ethyl acetate-hexane (2:7, v/v)-eluted fraction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06924300B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-a211681622b440f9a0339795514db2f4
출처 메모uspto-grants-2005_08