Reaktion #1483125

ord-f20999db59ab4d6091d7d696ee33cec5

Reaktionsgleichung

O=c1c(O)c(O)c1=O
squaric acid
CC(=O)Nc1cccc(N(C)CCO)c1
2-(methyl(3-acetaminophenyl)amino)ethan-1-ol
CCCCO
n-BuOH
CC(=O)Nc1cc(N(C)CCO)ccc1C1=C(O)C(c2ccc(N(C)CCO)cc2NC(C)=O)=C1O
desired compound
CC(=O)Nc1cc(N(C)CCO)ccc1C1=C(O)C(c2ccc(N(C)CCO)cc2NC(C)=O)=C1O
2,4-bis(2-acetamino-4-((2-hydroxyethyl)(methyl)amino)phenyl)cyclobuta-1,3-dien-1,3-diol

Lösungsmittel

Reaktionsbedingungen

Temperatur
120°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was heated
  2. 2
    Sonstigeto remove water
  3. 3
    Sonstigegenerated from the reactant during the reaction
  4. 4
    Sonstigethe reactant kept being reacted
  5. 5
    Temperaturthe reactant was cooled down
  6. 6
    Sonstigeproducing crystals
  7. 7
    FiltrationThe crystals were filtered
  8. 8
    Sonstigeonce more recrystallized

Vorschrift

342 mg of squaric acid) and 2 g of 2-(methyl(3-acetaminophenyl)amino)ethan-1-ol were put in a 100 mL 3-neck rounded bottom flask, and 40 mL of n-BuOH and 20 mL of toluene were added thereto. The mixture was heated and refluxed at 120° C. for 10 hours. Then, a Dean-Stark trap set was used to remove water generated from the reactant during the reaction, and the reactant kept being reacted. When the reaction was complete, the reactant was cooled down, producing crystals. The crystals were filtered, several times cleaned with hexane, and once more recrystallized, obtaining a desired compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08900780B2uspto-grants-2014_12