4-Bromotriphenylamine → HCID 57796676, compound

HRID 2099954Notes

Reaction equation

Br[C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][C:8]([Br:15])=[CH:9][CH:10]=3)[C:5]([CH2:18][CH3:19])([CH2:16][CH3:17])[C:4]=2[CH:3]=1.BrC1C=CC([N:25]([C:32]2[CH:37]=[CH:36][CH:35]=CC=2)[C:26]2C=CC=CC=2)=CC=1>>[Br:15][C:8]1[CH:7]=[C:6]2[C:11]([C:12]3[CH:13]=[CH:14][C:2]([C:35]4[N:25]([CH3:26])[CH:32]=[CH:37][CH:36]=4)=[CH:3][C:4]=3[C:5]2([CH2:18][CH3:19])[CH2:16][CH3:17])=[CH:10][CH:9]=1

Participants

Reactant 2

HCID 6428384-Bromotriphenylamine

HCID 35310452,7-Dibromo-9,9-diethylfluorene

Product 1

HCID 57796676HCID 57796676, compound

Procedure

The compound of the present example was synthesized by the same method as described in example 1, except that 3.80 parts of 2,7-dibromo-9,9-diethyl-9H-fluorene (21) was used to substitute 4-bromo-N,N-diphenylaniline.

Sources & evidence

ORD record: ord-077ac9bf96514dbe8ddee9efd6220d69
Source dataset: uspto-grants-2009_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07569704B1

Reaction notes

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