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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587740Generated: October 31, 2026

1,3-Dimethyl-2-imidazolidinone → HCID 136331481, compound

https://huagongshe.com/reaction/1587740

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
Reactantp-AminoacetophenoneHCID 7468—
ReactantEthylorthoformateHCID 53630039—
ReactantN-nitroimidazolidin-2-imineHCID 135413413—
CatalystSulfuric AcidHCID 1118—
SolventEthyl AcetateHCID 8857—
ProductHCID 136331481HCID 13633148153%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 5.0 g of p-aminoacetophenone. 6.6 g of ethyl orthoformate, 5 ml of 1,3-dimethyl-2-imidazolidinone and 0.03 g of concentrated sulfuric acid was placed in a reactor equipped with Dean's stark tube and agitated at 140° C. for about 10 minutes, followed by further addition of 5.8 g of nitroiminoimidazolidine and agitation at 160° C. for 1 hour. 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, and dried to give 5.4 g of 1-(4-methylcarbonyl-phenyliminomethyl)-2-nitroiminoimidazolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05219868
Source datasetuspto-grants-1993_06
ORD IDord-892d5c7f0fc544b9b232cf07c8a14e7f
Source noteuspto-grants-1993_06