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Isoprene → Isoprene acrylonitrile

HRID 595619
Notes
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Reaction equation

HRID 595619 reaction equation
[CH2:1]=[CH:2][C:3](=[CH2:5])[CH3:4].Cl[CH:7]([CH3:10])[C:8]#[N:9]>>[CH2:1]=[CH:2][C:3](=[CH2:4])[CH3:5].[C:8](#[N:9])[CH:7]=[CH2:10]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6557IsopreneHCID 5192252-Chloropropionitrile

Product 1

HCID 168239Isoprene acrylonitrile

Conditions

Temperature
80 °C

Procedure

Then, were added thereto 68.2 parts of isoprene and 1.79 parts of 2-chloropropionitrile as an organic halide, and stirred under heating at 80° C. to conduct a polymerization reaction. After 114 hours, the glass reaction vessel was cooled in a dry ice-methanol bath, and the volatiles were distilled off under reduced pressure to give a random (isoprene/acrylonitrile) copolymer. The conversion rate of isoprene was 84% and the conversion rate of acrylonitrile was 76%. The analysis results of the random (isoprene/acrylonitrile) polymer obtained are shown in Table 5. The polymer was confirmed to have a chlorine atom at the terminal of the polymer chain.

Workup

addition
Then, were added
  • customa polymerization reaction
  • customthe glass reaction vessel
  • temperaturewas cooled in a dry ice-methanol bath
  • distillationthe volatiles were distilled off under reduced pressure
  • Sources & evidence

    ORD record
    ord-b0f0ba87453446eb9351091f6ec32957
    Source dataset
    uspto-grants-2016_01
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US09243100B2

    Reaction notes

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    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes