N,N-dimethyl-p-phenylenediamine → HCID 23506685, compound

HRID 2086549Notes

Reaction equation

HRID 2086549 reaction equation
[ClH:1].[NH2:2][C:3]1[N:8]=[C:7]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([NH:16][C:17]2[CH:22]=[C:21](C(C)(C)C)[C:20](O)=[C:19](C(C)(C)C)[CH:18]=2)=[O:15])[CH:6]=[C:5]([CH3:32])[CH:4]=1.[CH3:33][N:34](C)[C:35]1C=CC(N)=CC=1.C(C1C=C(N)C=C(C(C)(C)C)C=1O)(C)(C)C>>[ClH:1].[NH2:2][C:3]1[N:8]=[C:7]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([NH:16][C:17]2[CH:18]=[CH:19][C:20]([N:34]([CH3:35])[CH3:33])=[CH:21][CH:22]=2)=[O:15])[CH:6]=[C:5]([CH3:32])[CH:4]=1

Participants

4

Reactant 3

HCID 7472N,N-dimethyl-p-phenylenediamineHCID 3142204-Amino-2,6-di-tert-butylphenolHCID 23506709HCID 23506709, compound

Product 1

HCID 23506685HCID 23506685, compound

Procedure

The experimental protocol used is the same as that described for compound 17, N,N-dimethyl-p-phenylenediamine replacing the 2,6-di-t-butyl-4-aminophenol. Hygroscopic grey solid.

Sources & evidence

ORD record
ord-cff6244289704eb69a02dc62539da1a6
Source dataset
uspto-grants-2004_04
Patent number
US06727239B1

Reaction notes

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