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

HRID 2083432Notes

Reaction equation

HRID 2083432 reaction equation
[CH2:1](N)[CH2:2]N>CO>[CH2:1]=[CH:2][CH:1]=[CH2:2].[CH2:1]=[CH:2][C:2]1[CH:1]=[CH:1][CH:2]=[CH:1][CH:2]=1

Participants

3

Procedure

The inside of the system with a 2 lit. capacity autoclave of stainless steel was fully purged with nitrogen gas and 985 cc of toluene, 13 cc of tetrahydrofuran, 135 cc of styrene, 900 cc of butadiene and 10 cc of a butyl lithium solution were put in the autoclave. The mixture solution thus formed was reacted at 70° C. for 3 hr. After sampling of a part of the reaction mixture solution in an amount of 100 cc, 25 g of ethylenediamine was added to the remaining solution to perform a further isomerization reaction. The isomerization reaction was carried out for another 6 hr at the temperature. And after the completion of the reaction, 40 cc of methanol was added thereto to inactivate the catalyst, followed by washing with water. The washing was repeated until the solution was not alkaline. By distilling off the solvents, there was obtained a butadiene-styrene copolymer in a pale color.

Workup

  1. customThe inside of the system with a 2 lit. capacity autoclave of stainless steel was fully purged with nitrogen gas and 985 cc of toluene, 13 cc of tetrahydrofuran, 135 cc of styrene, 900 cc of butadiene and 10 cc of a butyl lithium solution
  2. customThe mixture solution thus formed
  3. customwas reacted at 70° C. for 3 hr
  4. additionwas added to the remaining solution
  5. customa further isomerization reaction
  6. customThe isomerization reaction
  7. additionwas added
  8. washby washing with water
  9. distillationBy distilling off the solvents

Sources & evidence

ORD record
ord-eabd8bd7bbaf44d190fae574017956a6
Source dataset
uspto-grants-1978_04
Patent number
US04085263

Reaction notes

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