4-Bromotriphenylamine → HCID 57796691, compound

HRID 2099956Notes

Reaction equation

HRID 2099956 reaction equation
BrC1C=C[C:5]2[N:6]([CH2:16]CCCCC)[C:7]3[C:12]([C:13]=2C=1)=CC(Br)=CC=3.[Br:22][C:23]1[CH:41]=[CH:40][C:26]([N:27]([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[CH:25][CH:24]=1>>[CH3:16][N:6]1[CH:7]=[CH:12][CH:13]=[C:5]1[C:37]1[CH:36]=[C:35]2[C:34](=[CH:39][CH:38]=1)[N:27]([CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[C:26]1[CH:25]=[CH:24][C:23]([Br:22])=[CH:41][C:40]2=1

Participants

3

Reactant 2

HCID 6428384-BromotriphenylamineHCID 121742819H-Carbazole, 3,6-dibromo-9-hexyl-

Product 1

HCID 57796691HCID 57796691, compound

Procedure

The compound of the present example was synthesized by the same method as described in example 1, except that 4.09 parts of 3,6-dibromo-9-hexyl-9H-carbazole (31) was used to substitute 4-bromo-N,N-diphenyl aniline.

Sources & evidence

ORD record
ord-799e6a5aec0649a79a192edf42ec0908
Source dataset
uspto-grants-2009_08
Patent number
US07569704B1

Reaction notes

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