Reacción #1761

ord-d53ccc1fdb224edc9a97f3bf1af38c7c

Ecuación de reacción

NC(N)=O
urea
CN(C)c1ccc(C(O)C(=O)c2ccccc2)cc1
2-(4-dimethylaminophenyl)-2-hydroxy-1-phenylethanone
CN(C)c1ccc(-c2[nH]c(=O)[nH]c2-c2ccccc2)cc1
4-(4-dimethylaminophenyl)-2,3-dihydro-5-phenyl-1H-imidazol-2-one

Disolventes

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe reaction was cooled to ambient temperature
  2. 2
    FiltraciónThe resulting solid was filtered
  3. 3
    Lavadowashed with ether
  4. 4
    Otrodried in vacuo

Procedimiento

To acetic acid (2 mL) was added urea (0.6 g, 10 mmol) and 2-(4-dimethylaminophenyl)-2-hydroxy-1-phenylethanone (2.6 g, 10 mmol). After stirring for 2 hours at 120° C., the reaction was cooled to ambient temperature. The resulting solid was filtered, washed with ether, and dried in vacuo to give 4-(4-dimethylaminophenyl)-2,3-dihydro-5-phenyl-1H-imidazol-2-one; NMR (CDCl3) 10.98 (s,2), 7.5 (m,4), 7.4 (m,5), 3.18 (s,6) ppm.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726198uspto-grants-1998_03