Azobisisobutyronitrile → Naphthalene

HRID 1638125Notes

Reaction equation

HRID 1638125 reaction equation
[CH3:1][C:2]1[CH2:7][C:6](Cl)(C)[CH:5](Cl)[CH2:4][C:3]=1/[CH:11]=[CH:12]/Cl.[CH:14]1C=C(CN)C=C(CN)C=1.CC(N=NC(C#N)(C)C)(C#N)C>>[CH:1]1[C:2]2[C:3](=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH:11]=[CH:12][CH:14]=1

Participants

4

Reactant 3

HCID 6547AzobisisobutyronitrileHCID 151331,3-BenzenedimethanamineHCID 5458653HCID 5458653, compound

Product 1

HCID 931Naphthalene

Procedure

A laminate-type organic electrophotographic photoreceptor was produced in the same manner and in the same ratios of starting materials as in Example 24 except that (PC-1) was replaced by (PC-2), MXDA by azobisisobutylonitrile (AIBN), and the conditions of the reaction after the drying were changed to 120° C., 1 hour.

Workup

  1. customthe conditions of the reaction after the drying

Sources & evidence

ORD record
ord-9cc39c8b0cf746b29b0812cdad7853b9
Source dataset
uspto-grants-2000_03
Patent number
US06043334

Reaction notes

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