Reaktion #1483128

ord-07bc462f17ac4e93b274bb770155c413

Reaktionsgleichung

O=c1c(O)c(O)c1=O
squaric acid
C=CC(=O)Oc1cccc(N(C)CCO)c1
2-(methyl(3-acryloxyphenyl)amino)ethan-1-ol
CCCCO
n-BuOH
C=CC(=O)Oc1cc(N(C)CCO)ccc1C1=C(O)C(c2ccc(N(C)CCO)cc2OC(=O)C=C)=C1O
desired compound
C=CC(=O)Oc1cc(N(C)CCO)ccc1C1=C(O)C(c2ccc(N(C)CCO)cc2OC(=O)C=C)=C1O
2,4-bis(2-acryloxy-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 during the reaction
  4. 4
    Sonstigekept 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 2.12 g of 2-(methyl(3-acryloxyphenyl)amino)ethan-1-ol were put in a 100 mL 3-necked round 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 7 hours. Next, a Dean-Stark trap set was used to remove water generated during the reaction and 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