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Diethyl 5-hydantoylphosphonate → 5-[[2-Nitro-5-(1-piperidinyl)phenyl]methylene]-2,4-imidazolidinedione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl 5-hydantoylphosphonate | HCID 3516088 | — |
| 反応物 | 2-Nitro-5-(1-piperidinyl)benzaldehyde | HCID 3666345 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-[[2-Nitro-5-(1-piperidinyl)phenyl]methylene]-2,4-imidazolidinedione | HCID 54401842 | 92.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04701459 |
| 出典データセット | uspto-grants-1987_10 |
| ORD ID | ord-64c4743868ce4eb89eefe501ccd67221 |
| 出典メモ | uspto-grants-1987_10 |