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HRID 867477作成日:2026年10月25日

Potassium Carbonate → 5-[[5-[3-(2-Methyl-1,3-dioxolan-2-yl)propoxy]-2-nitrophenyl]methylene]-2,4-imidazolidinedione

https://huagongshe.com/reaction/867477

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物5-Hydroxy-2-nitrobenzaldehydeHCID 39211—
反応物2-(3-Chloropropyl)-2-methyl-1,3-dioxolaneHCID 80079—
反応物Sodium ethoxideHCID 2723922—
反応物Diethyl 5-hydantoylphosphonateHCID 3516088—
触媒Potassium IodideHCID 4875—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物5-[[5-[3-(2-Methyl-1,3-dioxolan-2-yl)propoxy]-2-nitrophenyl]methylene]-2,4-imidazolidinedioneHCID 5373424084%

反応条件

温度120 °C

反応手順

A mixture of 5-hydroxy-2-nitrobenzaldehyde (20.00 g, 0.12 mole), 5-chloro-2-pentanone ethylene ketal (21.7 g, 0.132 mole), potassium carbonate (20.00 g, 0.14 mole), potassium iodide (0.5 g) and dimethylformamide (200 mL) was heated with stirring at 120° C. After 4 hours, the mixture was cooled, diluted with water and extracted with diethyl ether. The combined ethereal extracts were washed with water, dried over magnesium sulfate and the solvent evaporated. The residual oil comprised of 5-[3-(2-methyl-1,3-dioxolan-2-yl)propoxy]-2-nitrobenzaldehyde (used without purification) was dissolved in ethanol (200 mL) and added in one portion to a solution of sodium ethoxide (10.05 g, 0.15 mole) and diethyl 2,4-dioxoimidazolidine-5-phosphonate (35.00 g, 0.15 mole) in ethanol (300 mL). The mixture was stirred at room temperature for 90 minutes, concentrated to a volume of approximate 300 mL and diluted with water. The yellow precipitate was filtered off, washed with water and dried in vacuo at 70° C. to give 5-[[5-[3-(2-methyl-1,3dioxolan-2-yl)propoxy]-2-nitrophenyl]methylene]-2,4-imidazolidinedione (38.01 g, 84%). An analytical sample was prepared by crystallization from ethanol and had m.p. 175°-180° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04775674
出典データセットuspto-grants-1988_10
ORD IDord-a41578fc11134582b8daf973efe503b8
出典メモuspto-grants-1988_10