Ethylene → Ethylene/Vinyl Acetate Maleic Anhydride

HRID 1578195ノート

反応式

HRID 1578195 の反応式
[C:1](OCC)(=O)[CH:2]=C.[C:8]1(=[O:14])[O:13][C:11](=[O:12])[CH:10]=[CH:9]1.C(OCC=C)(=O)C=C.N(C(C)(C)C#N)=NC(C)(C)C#N.B(F)(F)F.C=C>CC(C)=O.C(Cl)Cl>[CH2:1]=[CH2:2].[C:11]([O:13][CH:8]=[CH2:9])(=[O:12])[CH3:10].[C:11]1(=[O:12])[O:13][C:8](=[O:14])[CH:9]=[CH:10]1

参加物

9

反応物 6

HCID 6325Ethylene2 回HCID 6356Boron trifluorideHCID 6547AzobisisobutyronitrileHCID 7923Maleic AnhydrideHCID 8821Ethyl AcrylateHCID 13835Allyl acrylate

生成物 1

HCID 86650683Ethylene/Vinyl Acetate Maleic Anhydride

試薬・触媒・溶媒 2

HCID 180Acetone溶媒HCID 6344Dichloromethane溶媒

実験手順

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 1 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.

後処理

  1. additionwas charged under nitrogen with 4000 ml
  2. customIt was then sealed
  3. customThe subsequent copolymerization at 25° C.
  4. customabout two hours
  5. customThe reaction was quenched by addition of 1 liter of diethyl ether
  6. customVolatiles were removed by steam-stripping in a well-ventilated hood
  7. customThe terpolymer thereby obtained
  8. customprecipitated in water in a blender
  9. customoven-dried

出典と根拠

ORDレコード
ord-93f3a203a5eb4cfc973ea945ae24325d
出典データセット
uspto-grants-1981_09
特許番号
USRE030754

反応ノート

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