p-Toluenesulfonic acid → HCID 178448989, compound
Reaction equation
[F:1][C:2]1[CH:9]=[C:8]([O:10][CH3:11])[CH:7]=[C:6]([F:12])[C:3]=1[CH:4]=O.[CH2:13]([NH2:17])[CH2:14][CH2:15][CH3:16].C1(C)C=CC(S(O)(=O)=O)=CC=1>>[CH2:13](/[N:17]=[CH:4]/[C:3]1[C:2]([F:1])=[CH:9][C:8]([O:10][CH3:11])=[CH:7][C:6]=1[F:12])[CH2:14][CH2:15][CH3:16]Participants
4
Procedure
Butyl-[1-(2,6-difluoro-4-methoxy-phenyl)-meth-(E)-ylidene]-amine was prepared from 2,6-difluoro-4-methoxybenzaldehyde, N-butylamine and p-toluenesulphonic acid in analogy to Example 186a): yellow oil; MS (ISP): 228.4 ([M+H]+, 100%).
Sources & evidence
- ORD record
- ord-89ca1caf69ef4874afa0b8ff8cae7330
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07875645B2
Reaction notes
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