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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546554Generated: October 25, 2026

Triethylamine → 3-(4-Tert-butylphenyl)-5,5-dimethyl-imidazolidine-2,4-dione

https://huagongshe.com/reaction/546554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Tert-butyl-4-isocyanatobenzeneHCID 2735695—
ReactantMethyl 2-aminoisobutyrate hydrochlorideHCID 13258034—
SolventTolueneHCID 1140—
Product3-(4-Tert-butylphenyl)-5,5-dimethyl-imidazolidine-2,4-dioneHCID 5762597279.6%

Reaction Steps

To a suspension of 15 g of 4-tert-butylphenyl-isocyanate in 200 mL of toluene are successively added 31.52 mL of triethylamine and 13.15 g of 2,2-dimethylglycine methyl ester hydrochloride. The reaction mixture is refluxed for 24 h, cooled to room temperature, poured into distilled water and extracted with ethyl acetate. The organic phase is washed successively with water and with saturated sodium chloride solution, dried over magnesium sulphate, filtered and concentrated under reduced pressure. The residue is taken up in diethyl ether and the solid formed is filtered off and dried to give 17.75 g of 3-(4-tert-butylphenyl)-5,5-dimethyl-imidazolidine-2,4-dione, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935819B2
Source datasetuspto-grants-2011_05
ORD IDord-d90c02ee6adf431e9a8831060f8eba9f
Source noteuspto-grants-2011_05