Reaction equation
[C:1]1(=[O:11])[O:6][C:4](=[O:5])[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.[CH3:12][N:13]([CH3:24])[C:14]1[CH:15]=[C:16]([CH:21]=[CH:22][CH:23]=1)[NH:17][C:18](=[O:20])[CH3:19]>>[C:18]([NH:17][C:16]1[CH:15]=[C:14]([N:13]([CH3:12])[CH3:24])[CH:23]=[CH:22][C:21]=1[C:4]([C:3]1[CH:7]=[CH:8][CH:9]=[CH:10][C:2]=1[C:1]([OH:6])=[O:11])=[O:5])(=[O:20])[CH3:19]Participants
3
Procedure
Condensation of phthalic anhydride and m-(dimethylamino)acetanilide by the method of part A of Example 1 affords 2-(2-acetamido-4-(dimethylamino) benzoyl)benzoic acid (II: Y'2 = CH3CONH, Y'4 = (CH3)2N, Z4 = Z'5 = Z'6 = Z7 = H).
Sources & evidence
- ORD record
- ord-e9c4f011add24eb99bcd160da9678329
- Source dataset
- uspto-grants-1977_06
- Patent number
- US04032527
Linked notes
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