4-Methylbenzenethiol → 4-Methyl-2-nitro-1-p-tolylsulfanyl-benzene
Reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5](OS(C(F)(F)F)(=O)=O)=[C:4]([N+:16]([O-:18])=[O:17])[CH:3]=1.[CH3:19][C:20]1[CH:25]=[CH:24][C:23]([SH:26])=[CH:22][CH:21]=1>>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:26][C:23]2[CH:24]=[CH:25][C:20]([CH3:19])=[CH:21][CH:22]=2)=[C:4]([N+:16]([O-:18])=[O:17])[CH:3]=1Participants
3
Procedure
The product from Example 4a (5.00 g, 17.53 mmol) was reacted with 4-methylthiophenol (2.17 g, 17.53 mmol) in place of thiophenol following the procedure from Example 1e for 18 h giving the crude title compound which was purified by silica gel column chromatography eluting with 5% EtOAc/hexane providing a solid (3.53 g, 78%).
Sources & evidence
- ORD record
- ord-684f7f3363c94935959883043de42a0f
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07763731B2
Reaction notes
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