N,N-dimethyl-p-phenylenediamine → HCID 23506687, compound

HRID 1883530Notes

Reaction equation

HRID 1883530 reaction equation
[ClH:1].[NH2:2][C:3]1[N:8]=[C:7]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]([NH:17][C:18]2[CH:23]=[C:22](C(C)(C)C)[C:21](O)=[C:20](C(C)(C)C)[CH:19]=2)=[O:16])[CH:6]=[C:5]([CH3:33])[CH:4]=1.[CH3:34][N:35](C)[C:36]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][CH2:14][C:15]([NH:17][C:18]2[CH:19]=[CH:20][C:21]([N:35]([CH3:36])[CH3:34])=[CH:22][CH:23]=2)=[O:16])[CH:6]=[C:5]([CH3:33])[CH:4]=1

Participants

4

Reactant 3

HCID 7472N,N-dimethyl-p-phenylenediamineHCID 3142204-Amino-2,6-di-tert-butylphenolHCID 23506728HCID 23506728, compound

Product 1

HCID 23506687HCID 23506687, compound

Procedure

The experimental protocol used is the same as that described for compound 16, N,N-dimethyl-p-phenylenediamine replacing the 2,6-di-t-butyl-4-aminophenol. Hygroscopic yellowish solid.

Sources & evidence

ORD record
ord-7c4f723692824392981af04fab0da7ef
Source dataset
uspto-grants-2004_07
Patent number
US06762176B1

Reaction notes

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