4-Methoxybenzenesulfonyl chloride → 3-(4-Methoxyphenylsulfonyl)-2-phenylbenzothiophene
Reaction equation
[C:1]1([C:7]2[S:8][C:9]3[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=3[CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:16][O:17][C:18]1[CH:23]=[CH:22][C:21]([S:24](Cl)(=[O:26])=[O:25])=[CH:20][CH:19]=1>>[CH3:16][O:17][C:18]1[CH:19]=[CH:20][C:21]([S:24]([C:11]2[C:10]3[CH:12]=[CH:13][CH:14]=[CH:15][C:9]=3[S:8][C:7]=2[C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)(=[O:26])=[O:25])=[CH:22][CH:23]=1Participants
3
Procedure
Acylation of 2-phenylbenzothiophene with 4-methoxybenzenesulfonyl chloride as described above gives 3-(4-methoxyphenylsulfonyl)-2-phenylbenzothiophene.
Sources & evidence
- ORD record
- ord-b0c6c242cade47a989308f103b2d69cb
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04117128
Reaction notes
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