Benzo(B)Thiophene → 1-(Benzo[b]thiophen-2-ylmethyl)-5-bromo-2-ethoxybenzene
Reaction equation
[CH:1]1[CH:2]=[CH:3][C:4]2[S:9][CH:8]=[CH:7][C:5]=2[CH:6]=1.[Br:10][C:11]1[CH:12]=[CH:13][C:14]([O:19][CH2:20][CH3:21])=[C:15]([CH:18]=1)[CH:16]=O>>[S:9]1[C:8]([CH2:16][C:15]2[CH:18]=[C:11]([Br:10])[CH:12]=[CH:13][C:14]=2[O:19][CH2:20][CH3:21])=[CH:7][C:5]2[CH:6]=[CH:1][CH:2]=[CH:3][C:4]1=2Participants
3
Procedure
Thianaphthene and 5-bromo-2-ethoxybenzaldehyde were treated in a manner similar to Reference Example 7 to give the target compound.
Workup
- customto give the target compound
Sources & evidence
- ORD record
- ord-f8ee6a18027a4fd0820495f34bd58dc7
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07943788B2
Reaction notes
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