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Azobisisobutyronitrile → Prop-2-enenitrile--ethenylbenzene (1/1)

HRID 501504
Notes
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Reaction equation

HRID 501504 reaction equation
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:9](#[N:12])[CH:10]=[CH2:11].CC(N=NC(C#N)(C)C)(C#N)C.P([O-])([O-])([O-])=O.[Ca+2].[Ca+2].[Ca+2].P([O-])([O-])([O-])=O>O>[CH2:11]=[CH:10][C:9]#[N:12].[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 6547AzobisisobutyronitrileHCID 7501StyreneHCID 7855AcrylonitrileHCID 24456Tricalcium Phosphate

Product 1

HCID 62696Prop-2-enenitrile--ethenylbenzene (1/1)

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

72 parts of styrene, 28 parts of acrylonitrile, and 120 parts of deionized water are mixed. To the mixture, 0.2 parts of azobisisobutylonitrile (AIBN), 0.4 parts of tricalcium phosphate and 0.2 parts of mercaptan-containing chain transfer agent are added. The resultant solution is heated to 80° C. for 90 minutes and kept for 180 minutes. The resultant is washed, dehydrated and dried to obtain styrene-acrylonitrile copolymer resin (SAN) in powder form.

Workup

  1. additionare added
  2. washThe resultant is washed
  3. customdried

Sources & evidence

ORD record
ord-89cfc22dadac4e29aac79744d92ae7de
Source dataset
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07772303B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes