Реакция #347393

ord-3398696e7fff45f99d56a131dadee296

Уравнение реакции

O=C1CNC(=O)N1.O=C1NC(c2ccccc2)(c2ccccc2)C(=O)N1CO
5,5-Diphenyl-3-hydroxymethyl-2,4-imidazolidine-dione imidazolidinedione
CC(Br)C(=O)Cl
2-bromopropionyl chloride
CC(Br)C(=O)OCN1C(=O)NC(c2ccccc2)(c2ccccc2)C1=O
3-(2'-Bromopropionyl )oxymethyl-5,5- diphenyl-2,4 -imidazolidinedione

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураby heating for 30 minutes on a 100°-110° C. oil bath
  2. 2
    ТемператураThe reaction mixture was cooled
  3. 3
    Экстракцияthe resultant solution was extracted with aqueous potassium carbonate
  4. 4
    Другоеdried
  5. 5
    Другоеcrystallized
  6. 6
    ДругоеThe product was obtained as a solid white substance (1 g, 34% ), m.p. 112°-115° C

Методика

5,5-Diphenyl-3-hydroxymethyl-2,4-imidazolidine-dione imidazolidinedione (2 g, 0.0071 tool) was dissolved in 2-bromopropionyl chloride (8.5 g, 5 ml, 0.05 mol) by heating for 30 minutes on a 100°-110° C. oil bath. The reaction mixture was cooled, 20 ml of ethyl ether were added, and the resultant solution was extracted with aqueous potassium carbonate, dried and then crystallized. The product was obtained as a solid white substance (1 g, 34% ), m.p. 112°-115° C. Anal. calc. for C19H17N2O4Br: C, 54.69; H, 4.11; N, 6.72; Br, 19.15. Found: C, 54.77; H, 4.15; N, 6.69; Br, 19.25. The product has the formula: ##STR1524##

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05525727uspto-grants-1996_06