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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847374Generated: October 25, 2026

1,3-Dimethyl-2-imidazolidinone → HCID 131717499, compound

https://huagongshe.com/reaction/847374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
ReactantOctafluorotolueneHCID 9906—
ReactantPotassium HydroxideHCID 14797—
ReactantDL-5 Chloro-6-ethyl-4-(alphaethyl-4-hydroxybenzylamino)pyrimidineHCID 131716268—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 131717499HCID 131717499111.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1 g of dl-5-chloro-6-ethyl-4-(α-ethyl-4-hydroxybenzylamino)pyrimidine, 1 g of perfluorotoluene, 0.24 g of powdery potassium hydroxide and 20 ml of 1,3-dimethyl-2-imidazolidinone (DMI) was heated under stirring at 70° C. for 8 hours. After completion of the reaction, the reaction mixture was poured into water, and extracted with toluene. The extract was washed with water, dried over anhydrous sodium sulfate and then toluene was evaporated under reduced pressure. The oily product obtained was isolated by column chromatography (Wako gel C-200, eluted with toluene:ethyl acetate=30:1) to give 1.5 g of the desired product as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05141941
Source datasetuspto-grants-1992_08
ORD IDord-fae56da5724e44ad83bde53adc3f8250
Source noteuspto-grants-1992_08