2-[4-(Dimethylamino)benzoyl]benzoic acid → HCID 20341671, compound

HRID 2050111Notes

Reaction equation

HRID 2050111 reaction equation
[CH3:1][N:2]([CH3:20])[C:3]1[CH:19]=[CH:18][C:6]([C:7]([C:9]2[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=2[C:11]([OH:13])=O)=[O:8])=[CH:5][CH:4]=1.[CH3:21][N:22]([CH3:36])[C:23]1[CH:35]=[CH:34][C:26]([NH:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[CH:25][CH:24]=1>>[CH3:20][N:2]([CH3:1])[C:3]1[CH:4]=[CH:5][C:6]([C:7]2([N:27]([C:26]3[CH:25]=[CH:24][C:23]([N:22]([CH3:36])[CH3:21])=[CH:35][CH:34]=3)[C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=3)[C:9]3[C:10](=[CH:14][CH:15]=[CH:16][CH:17]=3)[C:11](=[O:13])[O:8]2)=[CH:18][CH:19]=1

Participants

3

Procedure

Following a procedure similar to that described in Example 1 but employing 2.6 g of 2-[4-(dimethylamino)benzoyl]benzoic acid and 2.1 g of 4-(dimethylamino)-N-phenylaniline there was obtained 2.2 g of 3-[4-(dimethylamino)phenyl]-3-{[4-(dimethylamino)phenyl]phenylamino}phthalide, m.p. 163°-166° C. A toluene solution of the product contacted with acidic clay or phenolic resin developed a brown-colored image.

Sources & evidence

ORD record
ord-38d76af08c2143749dfebf5765af6efa
Source dataset
uspto-grants-1980_04
Patent number
US04200313

Reaction notes

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