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HRID 742266Erstellt: 26. Oktober 2026

N-Phenylglycine ethyl ester → 3-(3-Chloro-2-methylphenyl)-1-phenyl-2-thioxo-imidazolidin-4-one

https://huagongshe.com/reaction/742266

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Phenylglycine ethyl esterHCID 75190—
Edukt1-Chloro-3-isothiocyanato-2-methylbenzeneHCID 140504—
LösungsmittelChloroformHCID 6212—
Produkt3-(3-Chloro-2-methylphenyl)-1-phenyl-2-thioxo-imidazolidin-4-oneHCID 1896821633,5%

Reaktionsschritte

A mixture of N-phenyl glycine ethyl ester (8.95 g), 3-chloro-2-methylphenylisothiocyanate (9.18 g), and chloroform (200 mL) was heated at reflux for 18 hours. The solvent was evaporated to dryness. The residue was mixed with ethanol (150 mL), and triethyl amine (3 mL). The mixture was heated at reflux for 3 hours. The solvent was evaporated. The residue was dissolved in ethyl acetate (300 mL) and washed with 1N HCl (2×200 mL), then with water (200 mL). The organic phase was dried over anhydrous magnesium sulfate and evaporated to dryness. The residue was treated with diethyl ether. The solid was collected by filtration and air dried to give the title compound (5.3 g) as an off-white solid, m.p. 154°-156° C. Anal. Calcd. for. C16H13Cl N2O S: C, 60.66; H, 4.14; N, 8.84. Found: C, 60.48; H, 4.05; N, 8.76. Mass spectrum (+FAB, [M+H]+) m/z 317/319.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05554607
Quelldatensatzuspto-grants-1996_09
ORD IDord-094b8222c69d4b80aee177bd9ba4b72e
Quellennotizuspto-grants-1996_09