Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllantoinHCID 204—
ReactantSodium hydrideHCID 24758—
Reactant3-Iodobenzyl bromideHCID 2759361—
SolventDimethylformamideHCID 6228—
ProductN-[1-(3-Iodobenzyl)-2,5-dioxoimidazolidin-4-yl]ureaHCID 2186706113.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144908B2
Source datasetuspto-grants-2006_12
ORD IDord-eac4c456015e4dc8826cc4c4d40ecc2b
Source noteuspto-grants-2006_12