Thionyl Chloride → 5-chloromethyl-1-methyl-3-(4-trifluoromethyl-phenyl)-1H-pyrazole
Reaction equation
[CH3:1][N:2]1[C:6]([CH2:7]O)=[CH:5][C:4]([C:9]2[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:17])[F:16])=[CH:11][CH:10]=2)=[N:3]1.S(Cl)([Cl:21])=O>C(Cl)(Cl)Cl>[Cl:21][CH2:7][C:6]1[N:2]([CH3:1])[N:3]=[C:4]([C:9]2[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:17])[F:16])=[CH:11][CH:10]=2)[CH:5]=1Participants
4
Procedure
In analogy to the procedure described for example 1 b], [2-methyl-5-(4-trifluoromethyl-phenyl)-2H-pyrazol-3-yl]-methanol (example 3 b]) was reacted with thionyl chloride in chloroform to yield 5-chloromethyl-1-methyl-3-(4-trifluoromethyl-phenyl)-1H-pyrazole as yellow oil.
Sources & evidence
- ORD record
- ord-1d0c236f492c49f3a574327873b64317
- Source dataset
- uspto-grants-2007_09
- Patent number
- US07265149B2
Reaction notes
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