Thiophenol → Benzene, 1,3-bis(phenylthio)-
Reaction equation
[K].[C:2]1([SH:8])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[C:10]1[CH:15]=[CH:14][CH:13]=[C:12](Cl)[CH:11]=1>>[C:2]1([S:8][C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([S:8][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[CH:11]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Procedure
The thiophenol derivative and the halogenated aromatic compound are reacted under the reaction conditions described above, subjected to distillation under a reduced pressure as it is or after filtration, to obtain a polyphenyl thioether crude product fraction. For example, by the reaction between a potassium salt of thiophenol and m-dichlorobenzene, a m-bis(phenylmercapto)benzene crude product can be obtained as a fraction at 220° C.-230° C./5 Torr.
Sources & evidence
- ORD record
- ord-9ada6759069f487997484cc2a31a5688
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06586376B1
Reaction notes
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