4-(2-Chloro-4-nitrophenoxy)phenol → 4-(2-Chloro-4-nitrophenoxy)phenyl 2-(4-(5-trifluoromethyl-2-pyridyloxy)phenoxy)propionate
Reaction equation
Cl.[F:2][C:3]([F:24])([F:23])[C:4]1[CH:5]=[CH:6][C:7]([O:10][C:11]2[CH:22]=[CH:21][C:14]([O:15][CH:16]([CH3:20])[C:17](Cl)=[O:18])=[CH:13][CH:12]=2)=[N:8][CH:9]=1.[Cl:25][C:26]1[CH:39]=[C:38]([N+:40]([O-:42])=[O:41])[CH:37]=[CH:36][C:27]=1[O:28][C:29]1[CH:34]=[CH:33][C:32]([OH:35])=[CH:31][CH:30]=1>>[F:2][C:3]([F:24])([F:23])[C:4]1[CH:5]=[CH:6][C:7]([O:10][C:11]2[CH:22]=[CH:21][C:14]([O:15][CH:16]([CH3:20])[C:17]([O:35][C:32]3[CH:33]=[CH:34][C:29]([O:28][C:27]4[CH:36]=[CH:37][C:38]([N+:40]([O-:42])=[O:41])=[CH:39][C:26]=4[Cl:25])=[CH:30][CH:31]=3)=[O:18])=[CH:13][CH:12]=2)=[N:8][CH:9]=1Participants
3
Procedure
In Example 1-13, by using 2-(4-(5-trifluoromethyl-2-pyridyloxy)phenoxy)propionic acid chloride hydrochloride instead of 2-(4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)phenoxy)propionic acid chloride hydrochloride, and 4-(2-chloro-4-nitrophenoxy)phenol instead of 4-(4-nitrophenoxy)phenol, 4-(2-chloro-4-nitrophenoxy)phenyl 2-(4-(5-trifluoromethyl-2-pyridyloxy)phenoxy)propionate was obtained.
Sources & evidence
- ORD record
- ord-8fda4e0e4acf482e97cdd38d3e57ea83
- Source dataset
- uspto-grants-1990_12
- Patent number
- US04976773
Reaction notes
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