Styrene → HCID 86662486, compound

HRID 516194Notes

Reaction equation

HRID 516194 reaction equation
[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:9]=[CH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[CH2:17]=[CH:18][CH2:19][CH2:20][CH2:21][CH2:22][CH:23]=[CH2:24]>C1(C)C=CC=CC=1>[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:9]=[CH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[CH2:17]=[CH:18][CH2:19][CH2:20][CH2:21][CH2:22][CH:23]=[CH2:24]

Participants

5

Procedure

The polymerization reaction was conducted in a 300 ml stainless autoclave equipped with a mechanical stirrer. The reactor was initially charged with 50 ml of toluene, 5 ml of 1-octene, 5 ml of styrene, and various quantities of 1,7-octadiene (1.6 ml, 0.8 ml, 0.4 ml, 0.2 ml and 0.1 ml) in an argon filled dry-box. The reactor was then sealed and then moved from the dry box and purged with nitrogen gas at 30° C. About 0.101 g of TiCl3(AA) and 1 ml of AlCl2Et in 10 ml of toluene after sufficiently stirring were introduced under nitrogen pressure to initiate the polymerization. After about 1 hour, the reaction was terminated by adding 100 ml of dilute HCl solution in methanol to the reactor. The polymers were isolated by filtration and washed completely with methanol and dried under vacuum for about 8 hours. The 1-octene/styrene/1,7-octadiene terpolymers were completely soluble in common organic solvents, including toluene and decalin.

Workup

  1. customThe polymerization reaction
  2. customequipped with a mechanical stirrer
  3. customThe reactor was then sealed
  4. custompurged with nitrogen gas at 30° C
  5. additionwere introduced under nitrogen pressure
  6. customthe polymerization
  7. customthe reaction was terminated
  8. additionby adding 100 ml of dilute HCl solution in methanol to the reactor
  9. customThe polymers were isolated by filtration
  10. washwashed completely with methanol
  11. customdried under vacuum for about 8 hours

Sources & evidence

ORD record
ord-80691b8206cc434781e8c8de78c8433a
Source dataset
uspto-grants-2015_08
Patent number
US09109057B2

Reaction notes

Loading…