M-Cresol → HCID 11990481, compound
Reaction equation
C[O:2][C:3](=[O:20])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[NH:10][C:11](=[O:19])[C:12]1[CH:17]=[CH:16][C:15](I)=[CH:14][CH:13]=1.[CH:21]1[C:26]([OH:27])=[CH:25][CH:24]=[CH:23][C:22]=1[CH3:28]>>[C:22]1([CH3:28])[CH:23]=[CH:24][CH:25]=[C:26]([O:27][C:15]2[CH:16]=[CH:17][C:12]([C:11]([NH:10][C:5]3[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=3[C:3]([OH:2])=[O:20])=[O:19])=[CH:13][CH:14]=2)[CH:21]=1Participants
3
Procedure
In analogy to example 2,2-(4-m-Tolyloxy-benzoylamino)-benzoic acid was prepared from 2-(4-iodo-benzoylamino)-benzoic acid methyl ester [75541-84-3] and m-cresol. MS (m/e): 346.3 (M−H−, 100%).
Sources & evidence
- ORD record
- ord-2089bc920d9c4ff4aecd06226bb71527
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07989657B2
Reaction notes
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