Reacción #71319

ord-4510b094a1a449d5a79b8154bf4bf400

Ecuación de reacción

C=C(C)C(=O)OCCOc1ccccc1
phenoxyethyl methacrylate
C=C(C)C(=O)O
methacrylic acid
C=C(C)C(=O)OC
methyl methacrylate
C=C(C)C(=O)O.C=C(C)C(=O)OC.C=C(C)C(=O)OCCOc1ccccc1
phenoxyethyl methacrylate methyl methacrylate methacrylic acid
Rendimiento 162.8%

Condiciones de reacción

Temperatura
72°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroequipped with a stirrer and a cooling tube
  2. 2
    OtroInto the flask, A solution prepared
  3. 3
    workup.ADDITIONwas added dropwise to the flask over a period of 3 hours
  4. 4
    workup.ADDITIONAfter completion of the addition
  5. 5
    Otroa solution prepared
  6. 6
    workup.ADDITIONwas added into the flask
  7. 7
    Temperaturathe solution was heated at 78° C. for 4 hours
  8. 8
    OtroThe reaction solution thus obtained
  9. 9
    Otrowas reprecipitated twice in an excess amount of hexane
  10. 10
    Otrothe precipitated resin was dried

Procedimiento

88 g of methyl ethyl ketone was placed in a 1000-mL three-necked flask equipped with a stirrer and a cooling tube, and heated to 72° C. in a nitrogen atmosphere. Into the flask, A solution prepared by dissolving 0.85 g of dimethyl 2,2′-azobisisobutyrate, 50 g of phenoxyethyl methacrylate, 13 g of methacrylic acid, and 37 g of methyl methacrylate in 50 g of methyl ethyl ketone was added dropwise to the flask over a period of 3 hours. After completion of the addition, the reaction was continued for further one hour, and then a solution prepared by dissolving 0.42 g of dimethyl 2,2′-azobisisobutyrate in 2 g of methyl ethyl ketone was added into the flask, and the solution was heated at 78° C. for 4 hours. The reaction solution thus obtained was reprecipitated twice in an excess amount of hexane, and the precipitated resin was dried to obtain 96.5 g of a phenoxyethyl methacrylate/methyl methacrylate/methacrylic acid (copolymerization ratio [% by mass]=50/37/13) copolymer (resin dispersant P-1).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08536246B2uspto-grants-2013_09