HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221957Generated: October 25, 2026
Potassium Iodide → 1-(4-Nitrobenzyl)tetrahydropyrimidin-2-one
https://huagongshe.com/reaction/221957
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | 2(1H)-Pyrimidinone, tetrahydro- | HCID 74615 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Nitrobenzyl)tetrahydropyrimidin-2-one | HCID 12678601 | — |
Reaction Steps
To a solution of 3,4,5,6-tetrahydro-2-(1H)-pyrimidinone (4 g, 0.04 mol) in abs. DMF (50 mL) there were added potassium carbonate (5.5 g, approximately 0.04 mol), potassium iodide (3.3 g, 0.02 mol), and 4-nitrobenzyl bromide (8.6 g, 0.04 mol) at RT. The reaction mixture was stirred at 100° C. over a period of 2 h. Following cooling of the reaction mixture, it was added to ice water (500 mL). The precipitated solid matter was filtered off in vacuo and washed with a little acetyl (4×10 mL). The desired product 1-(4-nitrobenzyl)tetrahydropyrimidin-2-one (H) was obtained as yellow solid matter (3.5 g, 40% of theory) having a melting point of 150-162° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207182B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-ff9bddc7f43c4f3fb05a537dc4ecd76f |
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| Source note | uspto-grants-2012_06 |
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