Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867477Generated: October 25, 2026

Potassium Carbonate → HCID 53734240, compound

https://huagongshe.com/reaction/867477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Hydroxy-2-nitrobenzaldehydeHCID 39211—
Reactant2-(3-Chloropropyl)-2-methyl-1,3-dioxolaneHCID 80079—
ReactantSodium ethoxideHCID 2723922—
ReactantDiethyl 5-hydantoylphosphonateHCID 3516088—
CatalystPotassium IodideHCID 4875—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 53734240HCID 5373424084%

Reaction Conditions

Temperature120 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775674
Source datasetuspto-grants-1988_10
ORD IDord-a41578fc11134582b8daf973efe503b8
Source noteuspto-grants-1988_10