Réaction #833525

ord-dc8752a737e04cf8b0d74078c20211cf

Équation de réaction

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
Rendement 88.5%

Conditions de réaction

Température
60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    LavageThe ethyl acetate layer was washed with water
  2. 2
    Séchagedried over anhydrous magnesium sulfate
  3. 3
    AutreThe solvent was removed by distillation from the ethyl acetate layer
  4. 4
    Autreto obtain solids
  5. 5
    Autrere-precipitated

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07393569B2uspto-grants-2008_07