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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49392생성일: 2026년 10월 24일

Acetamide → Benzyl-{2-[4-(2-methyl-oxazol-4-yl)-phenoxy]-ethyl]-carbamate

https://huagongshe.com/ko/reaction/49392

반응식

참여 물질

역할이름HCID투입량
반응물AcetamideHCID 178—
반응물Benzyl-[2-(4-bromoacetylphenoxy)-ethyl]-carbamateHCID 12986050—
생성물Benzyl-{2-[4-(2-methyl-oxazol-4-yl)-phenoxy]-ethyl]-carbamateHCID 2058795158%

반응 조건

온도130 °C

반응 단계

Acetamide (2.95 g, 50.0 mmol) and benzyl-[2-(4-bromoacetylphenoxy)-ethyl]-carbamate (1.20 g, 3.06 mmol) were combined in a round-bottomed flask and heated to about 130° C. for about ninety minutes. The reaction mixture was then allowed to cool to room temperature, and the resulting orange solid was partitioned between ethyl acetate and water and extracted three times with ethyl acetate. The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting crude solid was purified by column chromatography (silica gel; methylene chloride to 10% ethyl acetate/methylene chloride) to afford 621 mg (58% yield) of the product as a white solid. LRMS ([M+H]+)=353.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706743B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-8dfdc29225db4d1a972001c5c77782a5
출처 메모uspto-grants-2004_03