Reaktion #833525

ord-dc8752a737e04cf8b0d74078c20211cf

Reaktionsgleichung

C=CC(=O)Cl
Acrylic acid chloride
CC(C(=O)O)c1ccc(OCCCCCCO)cc1
(4-(6-hydroxyhexyloxy)phenyl)propionic acid
CN(C)c1ccccc1
N,N-dimethylaniline
C1COCCO1
dioxane
C=CC(=O)OCCCCCCOc1ccc(C(C)C(=O)O)cc1
(4-(6-acryloyloxyhexyloxy)phenyl)propionic acid
Ausbeute 88.5%

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    WaschenThe ethyl acetate layer was washed with water
  2. 2
    Trocknendried over anhydrous magnesium sulfate
  3. 3
    SonstigeThe solvent was removed by distillation from the ethyl acetate layer
  4. 4
    Sonstigeto obtain solids
  5. 5
    Sonstigere-precipitated

Vorschrift

Acrylic acid chloride (74.3 g) was dropped for 10 minutes to a mixture of (4-(6-hydroxyhexyloxy)phenyl)propionic acid (200 g), N,N-dimethylaniline (100 g), BHT (0.3 g), and dioxane (1,000 mL). After stirring at 60° C. for 5 hours, the reaction mixture was poured into water and stirred with addition of ethyl acetate. The ethyl acetate layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed by distillation from the ethyl acetate layer to obtain solids. The solids were dissolved in toluene and poured into plenty of heptane and re-precipitated to obtain (4-(6-acryloyloxyhexyloxy)phenyl)propionic acid (AK2: 213 g). Melting point: 64° C. to 68° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07393569B2uspto-grants-2008_07