HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857125Generated: October 26, 2026
Allantoin → N-[1-(3-Iodobenzyl)-2,5-dioxoimidazolidin-4-yl]urea
https://huagongshe.com/reaction/857125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allantoin | HCID 204 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Iodobenzyl bromide | HCID 2759361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[1-(3-Iodobenzyl)-2,5-dioxoimidazolidin-4-yl]urea | HCID 21867061 | 13.6% |
Reaction Steps
Allantoin (1.58 g) was stirred with meta-iodobenzyl bromide (2.97 g) in DMF (25 ml) at 21° under nitrogen and sodium hydride (60% oil dispersion; 0.40 g) was added over 5 min. After 2 h the solution was partitioned between EtOAc and water and hydrochloric acid was added to give pH 3. The separated aqueous layer was extracted with more EtOAc and the combined organic layers were washed with water and brine twice. After drying (MgSO4), the solution was concentrated to 20 ml. After 1 h the solid was collected by filtration and washed with EtOAc. The residue was boiled with EtOAc (50 ml) and the slurry was allowed to cool. The solid was collected by filtration, washed with ethyl acetate and dried to give the title compound (0.507 g). LCMS RT=2.44 min
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07144908B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-eac4c456015e4dc8826cc4c4d40ecc2b |
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| Source note | uspto-grants-2006_12 |
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