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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218524Generated: October 26, 2026

Ethylenediamine → 1-Methyl-3-(2-methyl-4-nitrophenyl)tetrahydropyrimidin-2(1H)-one

https://huagongshe.com/reaction/218524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Iodo-5-nitrotolueneHCID 79225—
Reactant1-Methyltetrahydropyrimidin-2(1H)-oneHCID 12867748—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product1-Methyl-3-(2-methyl-4-nitrophenyl)tetrahydropyrimidin-2(1H)-oneHCID 59586703—

Reaction Conditions

Temperature110 °C

Reaction Steps

16.1 g (76.1 mmol) of potassium phosphate and 0.362 g (1.90 mmol) of copper(I) iodide are initially charged, and the apparatus is baked out and then flushed with argon. 10.0 g (38.1 mmol) of 1-iodo-2-methyl-4-nitrobenzene, 6.51 g (57.0 mmol) of 1-methyltetrahydropyrimidin-2(1H)-one and 0.394 g (3.80 mmol) of N,N′-dimethylenediamine in 200 ml of dioxane are added, and the mixture is stirred at 110° C. After 19 h, after cooling, the mixture is filtered with suction through kieselguhr and then washed three times with 100 ml of ethyl acetate. The solvent is removed under reduced pressure and the residue is purified by chromatography on silica gel (2:1→1:1 cyclohexane/ethyl acetate). This affords 5.94 g (63% of theory) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198267B2
Source datasetuspto-grants-2012_06
ORD IDord-ba33e8432fa84103a431bb4b22c92229
Source noteuspto-grants-2012_06