Isoprene → 2-Methylbuta-1,3-diene;styrene

HRID 2421452Notes

Reaction equation

HRID 2421452 reaction equation
[CH2:1]=[CH:2][C:3](=[CH2:5])[CH3:4].[CH2:6]=[CH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1>ClC1C=CC=CC=1>[CH2:1]=[CH:2][C:3](=[CH2:4])[CH3:5].[CH2:6]=[CH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

Participants

4

Procedure

In a globe box, a magnetic stirring bar was placed in a flask (100 ml) and then added with isoprene (1.022 g, 15.0 mmol), styrene (3.124 g, 30.0 mmol), and [Sc(CH2SiMe3)2 (PNP) (0.019 g, 0.025 mmol) in chlorobenzene solution (8 ml), followed by the addition of [Ph3C] [B(C6F5)4] (0.023 g, 0.025 mmol) in chlorobenzene solution (2 ml) and stirring at high-speed. There action proceeded while stirring for 5 hours at room temperature and was then terminated by the addition of methanol. The reaction solution was poured into 200 ml of a methanol solution containing small amounts of hydrochloric acid and butylhydroxyl toluene. The precipitated polymer product was separated by decantation, washed with methanol, and dried at 60° C., thereby obtaining 1.230 g of copolymer.

Workup

  1. customIn a globe box, a magnetic stirring bar was placed in a flask
  2. stirringwhile stirring for 5 hours at room temperature
  3. customwas then terminated by the addition of methanol
  4. additionThe reaction solution was poured into 200 ml of a methanol solution
  5. additioncontaining small amounts of hydrochloric acid and butylhydroxyl toluene
  6. customThe precipitated polymer product was separated by decantation
  7. washwashed with methanol
  8. customdried at 60° C.

Sources & evidence

ORD record
ord-c245a5b003694888b0afe197a213a636
Source dataset
uspto-grants-2011_06
Patent number
US07956141B2

Reaction notes

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