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HRID 256173作成日:2026年10月26日

Diethyl 5-hydantoylphosphonate → 5-[[2-Nitro-5-(1-piperidinyl)phenyl]methylene]-2,4-imidazolidinedione

https://huagongshe.com/reaction/256173

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl 5-hydantoylphosphonateHCID 3516088—
反応物2-Nitro-5-(1-piperidinyl)benzaldehydeHCID 3666345—
反応物SodiumHCID 5360545—
溶媒EthanolHCID 702—
生成物5-[[2-Nitro-5-(1-piperidinyl)phenyl]methylene]-2,4-imidazolidinedioneHCID 5440184292.9%

反応手順

Sodium (0.6 g, 0.026 g atom) was dissolved in absolute ethanol (200 mL) and diethyl 2,4-dioxoimidazolidine-5-phosphonate (6.0 g, 25 mmol) added. After 10 minutes, 2-nitro-5-(1-piperidinyl)benzaldehyde (5.0 g, 21 mmol) was added in one portion and the mixture stirred at room temperature for 5 hours. The yellow precipitate was filtered off, washed with water and dried in air to give 5-[[2-nitro-5-(1-piperidinyl)phenyl]methylene]-2,4-imidazolidinedione (6.17 g, 92%), m.p. 273°-276° C. A sample dried in vacuo in 110° C. had m.p. 280° C. (dec.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04701459
出典データセットuspto-grants-1987_10
ORD IDord-64c4743868ce4eb89eefe501ccd67221
出典メモuspto-grants-1987_10