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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 867477생성일: 2026년 10월 25일

Potassium Carbonate → HCID 53734240, 화합물

https://huagongshe.com/reaction/867477

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-Hydroxy-2-nitrobenzaldehydeHCID 39211—
반응물2-(3-Chloropropyl)-2-methyl-1,3-dioxolaneHCID 80079—
반응물Sodium ethoxideHCID 2723922—
반응물Diethyl 5-hydantoylphosphonateHCID 3516088—
촉매Potassium IodideHCID 4875—
용매EthanolHCID 702—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물HCID 53734240HCID 5373424084%

반응 조건

온도120 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04775674
출처 데이터셋uspto-grants-1988_10
ORD IDord-a41578fc11134582b8daf973efe503b8
출처 메모uspto-grants-1988_10