2,6-Dimethylquinoline → HCID 54284774, compound

HRID 1586624Notes

Reaction equation

HRID 1586624 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([CH3:12])[CH:6]=[CH:5]2.[C:13]1([CH3:35])[CH:18]=[CH:17][C:16]([N:19]([C:28]2[CH:33]=[CH:32][C:31]([CH3:34])=[CH:30][CH:29]=2)[C:20]2[CH:27]=[CH:26][C:23]([CH:24]=O)=[CH:22][CH:21]=2)=[CH:15][CH:14]=1>>[C:31]1([CH3:34])[CH:32]=[CH:33][C:28]([N:19]([C:20]2[CH:21]=[CH:22][C:23]([CH3:24])=[CH:26][CH:27]=2)[C:16]2[CH:17]=[CH:18][C:13]([CH:35]=[CH:12][C:7]3[CH:6]=[CH:5][C:4]4[C:9](=[CH:10][CH:11]=[C:2]([CH3:1])[CH:3]=4)[N:8]=3)=[CH:14][CH:15]=2)=[CH:29][CH:30]=1

Participants

3

Reactant 2

HCID 134142,6-DimethylquinolineHCID 1707014-(Bis(p-tolyl)amino)benzaldehyde

Product 1

HCID 54284774HCID 54284774, compound

Procedure

By using 14 g of 6-methylquinaldine and 25 g of p-di(p-tolyl)aminobenzaldehyde and in the same manner as in Synthetic Example 1 the compound 2-[p-di(p-tolyl)aminostyryl]-6-methylquinoline was obtained. The yield was 24 g and the melting point thereof was 200°-202.5° C. This compound may also be used satisfactorily as a charge transport substance.

Sources & evidence

ORD record
ord-83cda7ed0ffc46f69df42c4cd6a63dd6
Source dataset
uspto-grants-1993_06
Patent number
US05215842

Reaction notes

Loading…