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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587739Generated: October 29, 2026

1,3-Dimethyl-2-imidazolidinone → HCID 136331480, compound

https://huagongshe.com/reaction/1587739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
Reactant3,4-DimethylanilineHCID 7248—
ReactantEthylorthoformateHCID 53630039—
ReactantN-nitroimidazolidin-2-imineHCID 135413413—
CatalystSulfuric AcidHCID 1118—
SolventEthyl AcetateHCID 8857—
ProductHCID 136331480HCID 13633148044.5%

Reaction Steps

A mixture of 60.6 g of 3,4-dimethylaniline, 200 g of ethyl orthoformate and 0.05 g of sulfuric acid was placed in a reactor equipped with Dean's stark tube and agitated at 140° to 165° C. for about 1 hour. After concentration of the reaction solution under reduced pressure, 45 g of nitroiminoimidazolidine and 70 g of 1,3-dimethyl-2-imidazolidinone were added and agitated at 140° to 160° C. for 2 hours. The reaction mixture was poured into 200 ml of a saturated saline solution, to which 150 ml of ethyl acetate was added. The resultant crystals were collected by filtration, washed with ethyl acetate and dried to give 40.2 g of 1-(3,4-dimethylphenyliminomethyl)-2-nitroiminoimidazolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05219868
Source datasetuspto-grants-1993_06
ORD IDord-d3dc8dd5dc08468cafe7513ce07fc15f
Source noteuspto-grants-1993_06