5-Fluoro-2-methoxythiophenol → 3-Chloro-4-[(5-fluoro-2-methoxyphenyl)thio]phenyl methyl sulfone
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:9][CH3:10])=[C:6]([SH:8])[CH:7]=1.[CH3:11][S:12]([C:15]1[CH:20]=[CH:19][C:18](F)=[C:17]([Cl:22])[CH:16]=1)(=[O:14])=[O:13]>>[CH3:11][S:12]([C:15]1[CH:20]=[CH:19][C:18]([S:8][C:6]2[CH:7]=[C:2]([F:1])[CH:3]=[CH:4][C:5]=2[O:9][CH3:10])=[C:17]([Cl:22])[CH:16]=1)(=[O:14])=[O:13]Participants
3
Procedure
The subtitle compound was prepared by the method of example 1 step (ii) using the product from step (ii) and the product from example 7 step (ii), yield 0.8 g.
Sources & evidence
- ORD record
- ord-692b418472204aca95c0541854e8add4
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08003703B2
Reaction notes
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