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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Iodo-5-nitrotoluene | HCID 79225 | — |
| Reactant | 1-Methyltetrahydropyrimidin-2(1H)-one | HCID 12867748 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-Methyl-3-(2-methyl-4-nitrophenyl)tetrahydropyrimidin-2(1H)-one | HCID 59586703 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198267B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-ba33e8432fa84103a431bb4b22c92229 |
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| Source note | uspto-grants-2012_06 |
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