Реакция #324365

ord-8ddcf2cd89834c66bb4be89b8a8530c1

Уравнение реакции

[H][H]
hydrogen
O=C(O)c1cc(C(=O)O)c(C(=O)O)cc1C(=O)O
pyromellitic acid
[H][H]
hydrogen
[H][H]
hydrogen
[H][H]
hydrogen
O=C(O)C1CC(C(=O)O)C(C(=O)O)CC1C(=O)O
1,2,4,5-cyclohexanetetracarboxylic acid
Выход 85.1%

Растворители

Условия реакции

Температура
60°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияwas filtered while it
  2. 2
    Другоеto separate the catalyst
  3. 3
    КонцентрированиеThe filtrate was concentrated
  4. 4
    Другоеby evaporating water under reduced pressure
  5. 5
    Другоеa rotary evaporator
  6. 6
    Другоеto precipitate crystals
  7. 7
    ДругоеThe precipitated crystals were separated by solid-liquid separation at room temperature
  8. 8
    Другоеdried

Методика

A 5-L Hastelloy (HC22) autoclave was charged with 552 g of pyromellitic acid, 200 g of a catalyst, that is, rhodium carried on activated carbon, available from N.E. Chemcat Corporation, and 1,656 g of water. The inner atmosphere of the reactor was replaced with nitrogen gas under stirring. After replacing the inner atmosphere of the reactor with hydrogen gas, the hydrogen pressure in the reactor was adjusted to 5.0 MPa and the temperature was raised to 60° C. While maintaining the hydrogen pressure at 5.0 MPa, the reaction was allowed to proceed for 2 hours. Then, after replacing the hydrogen gas in the reactor with nitrogen gas, the reaction product solution taken out of the autoclave was filtered while it was still hot to separate the catalyst. The filtrate was concentrated by evaporating water under reduced pressure using a rotary evaporator to precipitate crystals. The precipitated crystals were separated by solid-liquid separation at room temperature and dried, thereby obtaining 481 g of 1,2,4,5-cyclohexanetetracarboxylic acid (yield: 85.0%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08642181B2uspto-grants-2014_02