반응 #56350

ord-64a9bf2ab9ad4033bab0329dec4fa910

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04225476uspto-grants-1980_09