Реакция #215919

ord-e359cecf8b6b4adaac3cdb70f28c3aa5

Уравнение реакции

CC(C)(C)c1cc(C=O)cc(C(C)(C)C)c1O
3,5-di-t-butyl-4-hydroxybenzaldehyde
O=C1CNC(=O)N1
hydantoin
CC(=O)O
acetic acid
CC(C)(C)c1cc(C=C2NC(=O)NC2=O)cc(C(C)(C)C)c1O
product
Выход 50.6%
CC(C)(C)c1cc(C=C2NC(=O)NC2=O)cc(C(C)(C)C)c1O
5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]2,4-imidazolidinedione
Выход 50.6%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураheated to reflux
  2. 2
    Фильтрацияthe precipitate is filtered off
  3. 3
    Промывкаrinsed with water three times
  4. 4
    Другоеdried
  5. 5
    ДругоеRecrystallization from acetonitrile

Методика

A mixture of 3,5-di-t-butyl-4-hydroxybenzaldehyde (7.0 g, 30 mmoles), hydantoin (3.0 g, 30 mmoles), μ-alanine (1.4 g, 16 mmoles), and acetic acid (40 ml) is stirred under an inert atmosphere and heated to reflux. After 48 hours the mixture is stirred into water (300 ml), and the precipitate is filtered off, rinsed with water three times, and dried. Recrystallization from acetonitrile gave the pure product (4.8 g), mp 251°-252° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05464856uspto-grants-1995_11