Azobisisobutyronitrile → HCID 86738184, compound

HRID 1660537Notes

Reaction equation

HRID 1660537 reaction equation
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH:3]=[CH:2]1.[CH3:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH:14]=[CH2:15].CC(N=NC(C#N)(C)C)(C#N)C>C1(C)C=CC=CC=1>[CH2:8]=[CH:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].[C:4]1(=[O:5])[O:6][C:1](=[O:7])[CH:2]=[CH:3]1

Participants

5

Reactant 3

HCID 6547AzobisisobutyronitrileHCID 7923Maleic AnhydrideHCID 81251-Octene

Product 1

HCID 86738184HCID 86738184, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

98 Grams of maleic acid anhydride, 112 g of octene-1, 800 g of toluene and 4 g of AIBN were stirred for 9 hours at 90° C. Subsequently the mixture was rotated to dryness, the unreacted starting material being evaporated in the process.

Workup

  1. custombeing evaporated in the process

Sources & evidence

ORD record
ord-51d090eb9e5f4de58cee4c9d2e5d9324
Source dataset
uspto-grants-1981_12
Patent number
US04308362

Reaction notes

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