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HRID 247226作成日:2026年10月25日

p-Aminoacetophenone → N-[4-(1-hydroxyiminoethyl)phenyl]-N'-bis(methoxycarbonyl)methylurea

https://huagongshe.com/reaction/247226

反応式

関与物質

役割名称HCID仕込み量
反応物p-AminoacetophenoneHCID 7468—
反応物Trimethyl orthoformateHCID 9005—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物Dimethyl isocyanatomalonateHCID 14876291—
溶媒PyridineHCID 1049—
溶媒TetrahydrofuranHCID 8028—
生成物N-[4-(1-hydroxyiminoethyl)phenyl]-N'-bis(methoxycarbonyl)methylureaHCID 86741886—

反応手順

A solution of 0.02 mol 4-aminoacetophenone in 40 mL THF if added dropwise to a solution of 0.02 mol of dimethyl isocyanatomalonate and 5 mL pyridine in 40 mL THF, and the reaction mixture is stirred for 3 hours. The solvent is then removed by rotary evaporator. The residue is dispersed in 50 mL CH3OH, and 0.022 hydroxylamine hydrochloride and 0.06 mol trimethyl orthoformate are added. The reaction mixture is heated to reflux for 10 hours. The solvent is removed by rotary evaporator. Addition of water to the residue results in formation of N-[4-(1-hydroxyiminoethyl)phenyl]-N'-bis(methoxycarbonyl)methylurea, which is then treated with NaOCH3 to adjust the pH to 10. The solution is heated to reflux for 2.5 hours, and the solvent is removed under vacuum. The residue is washed with cold water to yield the crude 3-[4-(1-hydroxyiminoethyl)phenyl]-5-methoxycarbonylhydantoin.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04705864
出典データセットuspto-grants-1987_11
ORD IDord-adcab2c90b9d4fa39e7676b8a03f3d0f
出典メモuspto-grants-1987_11