Polysubstituted pyridine salt compound and its preparation method
A kind of salt compound and compound technology, applied in the field of polysubstituted pyridine salt compound and preparation thereof
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Embodiment 1
[0006] Example 1: One of the polysubstituted pyridinium salt compounds, N-methyl-2,6-diiodide
[0007] Preparation of (trans-4-methoxystyryl)pyridinium salt
[0008] With 12.5 parts by weight of iodide N-methyl-2,6-lutidine salt, the corresponding compound of 20.4 parts by weight of aldehydes, p-methoxybenzaldehyde is dissolved in 158 parts by weight of methanol, stirring, reflux 4 hours, slow cooling, precipitated solids, the precipitated solids were recrystallized twice in methanol, each with 474 parts by weight of methanol, after twice recrystallized to obtain 23.1 parts by weight of the corresponding disubstituted pyridinium salt, N iodide -Methyl-2,6-bis(trans-4-methoxystyryl)pyridinium salt, yield 95.1%.
Embodiment 2
[0009] Example 2: The second compound of polysubstituted pyridinium salts, N-methyl-2,6-diiodide
[0010] Preparation of [trans-4-(N,N-dimethylamino)styryl]pyridinium salt
[0011] With 12.5 parts by weight of iodide N-methyl-2,6-lutidine salt, 22.4 parts by weight of the corresponding compound of aldehydes, p-dimethylaminobenzaldehyde is dissolved in 158 parts by weight of methanol, stirring, Reflux for 4 hours, cool slowly, and precipitate solids, and the precipitated solids are recrystallized twice in methanol, each time with 474 parts by weight of methanol, to obtain 24.6 parts by weight of the corresponding disubstituted pyridinium salt, orange-red crystal iodide N- Methyl-2,6-bis[trans-4-(N,N-dimethylamino)styryl]pyridinium salt, yield 96.2%.
Embodiment 3
[0012] Example 3: The third of polysubstituted pyridinium salt compounds, iodide N-methyl-2,6-bis(trans-
[0013] Preparation of ferrocenevinyl)pyridinium salt
[0014] With 12.5 parts by weight of iodide N-methyl-2,6-lutidine salt, 32.1 parts by weight of the corresponding compound of aldehydes, ferrocene formaldehyde was dissolved in 158 parts by weight of methanol, stirred, refluxed for 4 hours, Slowly cooling, solid is separated out, the solid that is separated out is recrystallized twice in methanol, each time with the methanol of 632 parts by weight, obtains the corresponding disubstituted pyridinium salt of 30.2 parts by weight, iodide N-methyl-2,6- Bis(trans-ferrocenevinyl)pyridinium salt, yield 94.2%.
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