化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1099541作成日:2026年10月27日
4-Chlorobenzaldehyde → (4Z)-4-(4-Chlorobenzylidene)-2-{4-[2-(4-methoxyphenyl)ethoxy]phenyl}-1,3-oxazol-5(4H)-one
https://huagongshe.com/reaction/1099541
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Chlorobenzaldehyde | HCID 7726 | — |
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | N-{4-[2-(4-Methoxyphenyl)ethoxy]benzoyl}glycine | HCID 66812093 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | (4Z)-4-(4-Chlorobenzylidene)-2-{4-[2-(4-methoxyphenyl)ethoxy]phenyl}-1,3-oxazol-5(4H)-one | HCID 66812056 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08143446B2 |
|---|
| 出典データセット | uspto-grants-2012_03 |
|---|
| ORD ID | ord-6ed5f4a708ff427188f3cc13939949a5 |
|---|
| 出典メモ | uspto-grants-2012_03 |
|---|