Styrene → HCID 86593707, compound

HRID 1648465Notes

Reaction equation

HRID 1648465 reaction equation
[CH2:1]=[CH:2][C:3](=[CH2:5])[CH3:4].[CH2:6]=[CH:7][CH:8]=[CH2:9].[CH2:10]=[CH:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[CH2:1]=[CH:2][C:3](=[CH2:4])[CH3:5].[CH2:10]=[CH:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[CH2:6]=[CH:7][CH:8]=[CH2:9].[CH2:1]=[CH:2][C:3]1[CH:4]=[CH:8][CH:7]=[CH:6][CH:5]=1

Participants

3

Procedure

In the same manner, there were conducted addition of 0.01 mole of lithium sec-butyl followed by polymerization at 60° C. for 60 minutes, addition of 200 g of a 50/50 by weight mixture of isoprene/butadiene followed by polymerization at 60° C. for 60 minutes and addition of 50 g of styrene followed by polymerization for 60 minutes, to obtain a styrene-isoprene/1,3-butadiene-styrene block copolymer. Hydrogenation was conducted in the same manner as above to obtain a block copolymer having a hydrogenation ratio of 98%. This was named SEEPS-1.

Workup

  1. customfollowed by polymerization at 60° C. for 60 minutes
  2. customfollowed by polymerization at 60° C. for 60 minutes
  3. customfollowed by polymerization for 60 minutes

Sources & evidence

ORD record
ord-5ec24761e14744c386fabbd482c7d683
Source dataset
uspto-grants-1995_07
Patent number
US05436295

Reaction notes

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