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HRID 49392作成日:2026年10月25日

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

https://huagongshe.com/reaction/49392

反応式

関与物質

役割名称HCID仕込み量
反応物AcetamideHCID 178—
反応物Benzyl-[2-(4-bromoacetylphenoxy)-ethyl]-carbamateHCID 12986050—
生成物Benzyl-{2-[4-(2-methyl-oxazol-4-yl)-phenoxy]-ethyl]-carbamateHCID 2058795158%

反応条件

温度130 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706743B2
出典データセットuspto-grants-2004_03
ORD IDord-8dfdc29225db4d1a972001c5c77782a5
出典メモuspto-grants-2004_03