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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Chlorobenzaldehyde | HCID 7726 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 반응물 | N-{4-[2-(4-Methoxyphenyl)ethoxy]benzoyl}glycine | HCID 66812093 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | (4Z)-4-(4-Chlorobenzylidene)-2-{4-[2-(4-methoxyphenyl)ethoxy]phenyl}-1,3-oxazol-5(4H)-one | HCID 66812056 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08143446B2 |
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| 출처 데이터셋 | uspto-grants-2012_03 |
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| ORD ID | ord-6ed5f4a708ff427188f3cc13939949a5 |
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| 출처 메모 | uspto-grants-2012_03 |
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