Реакция #40924

ord-ef3281565b4e4622afcb19c9b901291b

Уравнение реакции

O=C1C=CC(=O)N1
Maleimide
Nc1ccc(C(F)(F)F)cc1
4-(trifluoromethyl)aniline
O=N[O-].[Na+]
sodium nitrite
CC(=O)[O-].[Na+]
sodium acetate
Cl
hydrochloric acid
O=C1C=C(c2ccc(C(F)(F)F)cc2)C(=O)N1
title compound
Выход 69.0%
O=C1C=C(c2ccc(C(F)(F)F)cc2)C(=O)N1
3-[4-(trifluoromethyl)phenyl]-1H-pyrrole-2,5-dione
Выход 69.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGto stir for further 30 minutes
  2. 2
    Другоеwas reduced to 0° C.
  3. 3
    ДругоеAt the end of diazotisation, a clear yellow solution was obtained
  4. 4
    workup.WAITAfter a few minutes a gas started
  5. 5
    workup.STIRRINGto stir at 0° C. for 1 h and overnight at room temperature
  6. 6
    ДругоеAcetone was removed in vacuo
  7. 7
    Фильтрацияthe residue was filtered
  8. 8
    Другоеdried overnight in vacuo

Методика

A mixture of hydrochloric acid (37% in water, 285 mL) and water (190 mL) was added to 4-(trifluoromethyl)aniline (150 g, 116 mL) at room temperature with vigorous stirring and the formed precipitate was allowed to stir for further 30 minutes. Temperature was reduced to 0° C. and sodium nitrite (70.6 g) in 180 mL of water was added dropwise to the stirred suspension. At the end of diazotisation, a clear yellow solution was obtained. Maleimide (180 g) in acetone (1.1 L) was added dropwise at 0° C. and then the pH of the solution was adjusted to 3-3.5 by adding sodium acetate. Copper (II) chloride (18.8 g) was added to the vigorously stirred mixture. After a few minutes a gas started to develop (conspicuous foaming). The reaction mixture was allowed to stir at 0° C. for 1 h and overnight at room temperature. Acetone was removed in vacuo, the residue was filtered and dried overnight in vacuo to give the title compound (155 g) as a light brown solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07727988B2uspto-grants-2010_06