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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416398Generated: November 3, 2026

Dioxoimidazolidine-3-acetate → 5-Hydroxy-1-(3-nitrobenzyl)-2,4-dioxoimidazolidine-3-acetic acid

https://huagongshe.com/reaction/1416398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDioxoimidazolidine-3-acetateHCID 2512551—
Reactant3-(3-Nitrobenzyl)-4,5-dioxo-2-thioxoimidazolidine-1-acetic acidHCID 10639626—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
Product5-Hydroxy-1-(3-nitrobenzyl)-2,4-dioxoimidazolidine-3-acetic acidHCID 10852365—

Reaction Steps

The above-prepared dioxoimidazolidine-3-acetate product of paragraph (2) (3.6 g) was dissolved in a mixed solvent of 4N hydrochloric acid and dioxane and the solution was stirred at room temperature for six hours. The reaction solution was concentrated in vacuo to dryness and then chloroform was added to the residue. The crystals were dislodged from the wall of the reaction flask with a spatula. The solid was collected by filtration, washed with chloroform and dried to give 0.8 g of 5-hydroxy-1-(3-nitrobenzyl)-2,4-dioxoimidazolidine-3-acetic acid [Compound 14] as amorphous crystals. The melting point, MS, IR, NMR, and elementary analysis for the compound were:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912261
Source datasetuspto-grants-1999_06
ORD IDord-d44e976853a54eb69ddafa30fea329b5
Source noteuspto-grants-1999_06