Reacción #56350

ord-64a9bf2ab9ad4033bab0329dec4fa910

Ecuación de reacción

C=CC(=O)OCC
ethyl acrylate
FB(F)F
boron trifluoride
C=CCOC(=O)C=C
allyl acrylate
CC(C)(C#N)N=NC(C)(C)C#N
azobis(isobutyronitrile)
C=C
ethylene
C=C
ethylene
O=C1C=CC(=O)O1
maleic anhydride
C=C.C=CC(=O)OCC.C=CCOC(=O)C=C.O=C1C=CC(=O)O1
Ethylene/Ethyl Acrylate Allyl Acrylate Maleic Anhydride

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas charged under nitrogen with 4000 ml
  2. 2
    OtroIt was then sealed
  3. 3
    OtroThe subsequent copolymerization at 25° C.
  4. 4
    Otroabout two hours
  5. 5
    OtroThe reaction was quenched by addition of one liter of diethyl ether
  6. 6
    OtroVolatiles were removed by steam-stripping in a well-ventilated hood
  7. 7
    OtroThe terpolymer thereby obtained
  8. 8
    Otroprecipitated in water in a blender
  9. 9
    Otrooven-dried

Procedimiento

A 7.57-liter stirred autoclave was charged under nitrogen with 4000 ml. of methylene chloride, 400 grams of ethyl acrylate, 20 grams of maleic anhydride, 1.2 grams of allyl acrylate, and 1.0 gram of azobis(isobutyronitrile). It was then sealed, charged with 300 grams of boron trifluoride, and pressured to 21 kg./sq. cm. with ethylene. The subsequent copolymerization at 25° C. was continued until pressure measurement indicated that ethylene uptake had ceased (about two hours later). The reaction was quenched by addition of one liter of diethyl ether. Volatiles were removed by steam-stripping in a well-ventilated hood. The terpolymer thereby obtained was dissolved in acetone, precipitated in water in a blender, and oven-dried. Yield: 415 grams.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04225476uspto-grants-1980_09