Benzyl Chloride → HCID 49824261, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9](=[O:16])[CH2:10][N:11]1[CH:15]=[N:14][CH:13]=[N:12]1.[CH2:17](Cl)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[Cl:8][C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[C:3]=1[C:9]([O:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[CH:10][N:11]1[CH:15]=[N:14][CH:13]=[N:12]1Participants
3
Procedure
Analogously to Example 1a,b, after reacting 1-(2,6-dichlorophenyl)-2-[1,2,4]triazol-1-yl-ethanone with benzyl chloride there was obtained 1-[2-(2,6-dichloro-phenyl)-2-benzyloxy-vinyl]-1H-[1,2,4]triazole. After reaction with oxalic acid there was obtained a salt with the composition C17H13N3OCl2.C2H2O4, which decomposed at >71° C.
Sources & evidence
- ORD record
- ord-8d595405f8304f9687b42e3b9c1baa8c
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06248901B1
Reaction notes
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