PHENYLACETIC ACID,2-(2'-CL-6-ME)ANILINO → 4-Nitrophenyl 2-(2,6-dichlorophenyl-amino)-phenyl-acetate
Reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([O:10][C:11](=[O:28])[CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[NH:19][C:20]2[C:21](C)=[CH:22][CH:23]=[CH:24][C:25]=2[Cl:26])=[CH:6][CH:5]=1)([O-:3])=[O:2].[Cl:29]C1C=CC=C(C)C=1NC1C=CC=CC=1CC(O)=O>>[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([O:10][C:11](=[O:28])[CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[NH:19][C:20]2[C:25]([Cl:26])=[CH:24][CH:23]=[CH:22][C:21]=2[Cl:29])=[CH:6][CH:5]=1)([O-:3])=[O:2]Participants
3
Procedure
[o-(3-chloro-o-toluidino)-phenyl]-acetic acid-p-nitrophenyl ester, starting with [o-(3-chloro-o-toluidino)-phenyl]-acetic acid, M.P. 124° - 125° (from ether/petroleum ether).
Sources & evidence
- ORD record
- ord-c0c6d8ee0b06401fa19c4f587510bbed
- Source dataset
- uspto-grants-1978_05
- Patent number