Styrene → HCID 86593707, compound
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]=1Participants
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
- customfollowed by polymerization at 60° C. for 60 minutes
- customfollowed by polymerization at 60° C. for 60 minutes
- customfollowed by polymerization for 60 minutes
Sources & evidence
- ORD record
- ord-5ec24761e14744c386fabbd482c7d683
- Source dataset
- uspto-grants-1995_07
- Patent number
- US05436295
Reaction notes
Loading…