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

HRID 453477
Notes
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Reaction equation

HRID 453477 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, 120 parts of deionized water and 0.2 parts of azobisisobutylonitrile (AIBN) are mixed. To the mixture, 0.4 parts of tricalciumphosphate 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 240 minutes. The resultant is washed, dehydrated and dried to obtain styrene-acrylonitrile copolymer resin (SAN) in powder form. The weight average molecular weight of the SAN copolymer resin is 180,000 to 200,000.

Workup

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

Sources & evidence

ORD record
ord-d6e3f2b2749f4d9bb43c6aceeff7878b
Source dataset
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08492463B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes