Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[F:9].[C:10]1([C:16]2[S:20][C:19]([CH:21]=O)=[CH:18][CH:17]=2)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>>[Br:1][C:2]1[C:3]([F:9])=[C:4]([CH2:21][C:19]2[S:20][C:16]([C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=3)=[CH:17][CH:18]=2)[C:5]([CH3:8])=[CH:6][CH:7]=1Participants
3
Procedure
4-Bromo-3-fluorotoluene and 5-phenyl-2-thiophenecarboxaldehyde were treated in a manner similar to Reference Example 116 to give the target compound as pale blue powders. APCI-Mass m/Z 361/363 (M+H).
Sources & evidence
- ORD record
- ord-59809dccd2824e33bf09d80dec4dcc27
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07943788B2
Linked notes
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