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HRID 231127作成日:2026年10月26日

Water → 4,5-Dihydro-4-oxo-N-phenyl-2-(phenylamino)-3-furancarboxamide

https://huagongshe.com/reaction/231127

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Phenyl isocyanateHCID 7672—
反応物Sodium hydrideHCID 24758—
反応物4-Bromo-3-oxo-n-phenylbutanamideHCID 268268—
溶媒1,4-DioxaneHCID 31275—
生成物4,5-Dihydro-4-oxo-N-phenyl-2-(phenylamino)-3-furancarboxamideHCID 14198535—

反応手順

Under a nitrogen atmosphere, sodium hydride (97%; 0.633 g, 25.61 mmol) was weighed into a dry reaction vessel and covered with 55 ml of anhydrous dioxane. A solution of phenyl isocyanate (1.39 ml, 12.81 mmol) in 5 ml of anhydrous dioxane was then added over a 5-10 minute period at room temperature (cooling with cold water). Next, the 4-bromoacetoacetanilide (3.28 g, 12.8 mmol) was added portionwise over a 20-minute period. The reaction mixture was stirred at 20°-25° C. for 5 hours, filtered under nitrogen atmosphere, and poured into 300 ml of ice-cold water. After acidifying (pH 5-6) with several drops of concentrated hydrochloric acid, the crude product was filtered off and crystallized from ethanol to provide 2.8 g. of amide product, m.p. 182°-184° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04845122
出典データセットuspto-grants-1989_07
ORD IDord-727b3696ee3c4956a2b6d68519769f7d
出典メモuspto-grants-1989_07