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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985176Generated: October 28, 2026

p-Xylyl bromide → [1-(4-Methyl-benzyl)-2,5-dioxo-imidazolidin-4-yl]-acetic acid methyl ester

https://huagongshe.com/reaction/1985176

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Xylyl bromideHCID 7721—
ReactantPotassium CarbonateHCID 11430—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantMethyl (2,5-dioxoimidazolidin-4-yl)acetateHCID 5296047—
SolventDimethylformamideHCID 6228—
Product[1-(4-Methyl-benzyl)-2,5-dioxo-imidazolidin-4-yl]-acetic acid methyl esterHCID 5771899197%

Reaction Steps

A solution of (2,5-dioxo-imidazolidin-4-yl)-acetic acid, methyl ester (2.35 g, 13.7 mmol) in DMF (100 mL) is treated with p-methyl benzyl bromide (2.90 g, 15.7 mmol), MgSO4 (3.30 g, 27.4 mmol) and then K2CO3 (3.77 g, 27.3 mmol). The resultant mixture is stirred under N2 in an ice bath for 30 minutes and then warmed to room temperature for 16 h. The reaction mixture is then filtered, and then aqueous 1N HCl (150 mL) is added to the filtrate. The filtrate is extracted with EtOAc and the organic layer dried. The solvent is removed to give 4.11 g crude product which is purified by flash chromatography using 100% CH2Cl2 then 97.5:2.5 CH2Cl2:MeOH to give 3.67 g (97%) [1-(4-methyl-benzyl)-2,5-dioxo-imidazolidin-4-yl]-acetic acid methyl ester. 1H NMR. MS (ES+) Calc'd for C14H17N2O4 (M+1) 277. Found m/z 277 (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544812B2
Source datasetuspto-grants-2009_06
ORD IDord-527ef5b1b0364256adb696464defa5be
Source noteuspto-grants-2009_06