Styrene → Benzene, ethenyl-, polymer with 1,3-butadiene

HRID 257123

反応式

HRID 257123 の反応式
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C=CC=C.CO.Cl>C[O-].C[O-].C[O-].C[Ti](C)(C)(C)(C)C1C=CC=C1.CO>[CH2:1]=[CH:2][CH:3]=[CH2:4].[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

参加物

6

反応条件

温度
30 °C

実験手順

In a 1.0-liter reactor equipped with a stirrer were placed 100 ml of styrene and 6.0 mmol as aluminum atom of methylaluminoxane obtained in the above Example 1 (1), and the resultant was stirred at the polymerization temperature of 30° C. for 30 minutes. Subsequently, 56.3 g of 1,3-butadiene was charged in a stainless steel catalyst-input tube which had been sufficiently replaced with nitrogen, and added to the reaction system, and, at the same time, 0.03 mmol as titanium atom of pentamethylcyclopentadienyltitanium trimethoxide was added. And polymerization was carried out at 40° C. for 5 hours with stirring. After reaction was over, methanol was poured to stop the reaction. Further, a mixture of methanol-hydrochloric acid was added to decompose the catalyst components. Then, washing with methanol was repeated three times. The yield of thus obtained styrene-1,3-butadiene copolymer was 41.4 g. Intrinsic viscosity measured in 1,2,4-trichlorobenzene at 135° C. was 1.63 dl/g.

後処理

  1. customIn a 1.0-liter reactor equipped with a stirrer
  2. additionadded to the reaction system
  3. customAnd polymerization
  4. waitwas carried out at 40° C. for 5 hours
  5. stirringwith stirring
  6. customAfter reaction
  7. additionwas poured
  8. customthe reaction
  9. additionwas added
  10. washThen, washing with methanol
  11. custommeasured in 1,2,4-trichlorobenzene at 135° C.

出典と根拠

ORDレコード
ord-2ae417eca07742adab0aef133d5937a5
出典データセット
uspto-grants-1993_11
特許番号
US05260394

関連ノート

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