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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1099541생성일: 2026년 10월 26일

4-Chlorobenzaldehyde → (4Z)-4-(4-Chlorobenzylidene)-2-{4-[2-(4-methoxyphenyl)ethoxy]phenyl}-1,3-oxazol-5(4H)-one

https://huagongshe.com/reaction/1099541

반응식

참여 물질

역할이름HCID투입량
반응물4-ChlorobenzaldehydeHCID 7726—
반응물Acetic AnhydrideHCID 7918—
반응물Sodium AcetateHCID 517045—
반응물N-{4-[2-(4-Methoxyphenyl)ethoxy]benzoyl}glycineHCID 66812093—
용매WaterHCID 962—
생성물(4Z)-4-(4-Chlorobenzylidene)-2-{4-[2-(4-methoxyphenyl)ethoxy]phenyl}-1,3-oxazol-5(4H)-oneHCID 6681205687%

반응 조건

온도120 °C

반응 단계

A mixture of N-{4-[2-(4-methoxyphenyl)ethoxy]benzoyl}glycine (329 mg, 1.00 mmol) prepared in Example 1 (1b), 4-chlorobenzaldehyde (148 mg, 1.05 mmol), sodium acetate (111 mg, 1.35 mmol), and acetic anhydride (467 μL, 5.00 mmol) was stirred at 120° C. for 20 minutes, and then water was added thereto to terminate the reaction. Then, continuously, the mixture was vigorously stirred until the mixture was cooled to room temperature. The deposited precipitate was collected by filtration, washed with water and hexane, and dried by heating under reduced pressure to give 376 mg of the title compound (yellow powder, yield: 87%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143446B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-6ed5f4a708ff427188f3cc13939949a5
출처 메모uspto-grants-2012_03