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HRID 456268作成日:2026年10月26日

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

https://huagongshe.com/reaction/456268

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChlorobenzaldehydeHCID 7726—
反応物Acetic AnhydrideHCID 7918—
反応物Sodium AcetateHCID 517045—
反応物N-{4-[2-(4-Methoxyphenyl)ethoxy]benzoyl}glycineHCID 66812093—
溶媒WaterHCID 962—
生成物(4Z)-4-(4-Chlorobenzylidene)-2-{4-[2-(4-methoxyphenyl)ethoxy]phenyl}-1,3-oxazol-5(4H)-oneHCID 6681205687%

反応条件

温度120 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08497397B2
出典データセットuspto-grants-2013_07
ORD IDord-3671a4b7833f475f8680cd21514b8701
出典メモuspto-grants-2013_07