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HRID 1944709作成日:2026年10月26日

Formamide → 4-Phenyl-1,3-oxazole

https://huagongshe.com/reaction/1944709

反応式

関与物質

役割名称HCID仕込み量
反応物FormamideHCID 713—
反応物Phenacyl bromideHCID 6259—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物4-Phenyl-1,3-oxazoleHCID 58927939.1%

反応条件

温度130 °C

反応手順

Bromoacetophenone (595 mg, 2.99 mmol) and formamide (1781 μl, 44.8 mmol) were combined and heated at 130° C. for 90 min. The reaction was cooled then dilute with ethyl acetate and water and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered, and concentrated. The concentrate was purified by chromatography on a Biotage 25M column using a 5-8% ethyl acetate in heptane gradiant to yield 4-phenyl-oxazole (170 mg, 1.17 mmol). TLC (5% ethyl acetate in heptane) of product: Rf=0.28.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08394858B2
出典データセットuspto-grants-2013_03
ORD IDord-052b546579ef47e1bf8a809b91d1baf8
出典メモuspto-grants-2013_03