Reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[SH:9].[Br:10][C:11]1[CH:16]=[C:15]([Br:17])[CH:14]=[CH:13][C:12]=1I.BrC1C=C(Br)C=CC=1N>>[Br:10][C:11]1[CH:16]=[C:15]([Br:17])[CH:14]=[CH:13][C:12]=1[S:9][C:3]1[CH:4]=[CH:5][C:6]([CH3:8])=[CH:7][C:2]=1[CH3:1]Participants
4
Procedure
Prepared from 2,4-dimethyl-benzenethiol and 2,4-dibromo-1-iodo-benzene (prepared from 2,4-dibromo-phenylamine by diazotization according to the general procedure by Tunney and Stille J. Org. Chem. 1987, 52, 748-753).
Sources & evidence
- ORD record
- ord-7151fd191b8149959cec8ccb108033bc
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07732463B2
Linked notes
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