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1236769-86-0

5-Allyl-2-chloro-3-fluoroisonicotinaldehyde synthesis

2synthesis methods
17282-04-1 Synthesis
2-Chloro-3-fluoropyridine

17282-04-1
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$7.00/10g

5-Allyl-2-chloro-3-fluoroisonicotinaldehyde

1236769-86-0
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Yield:1236769-86-0 41%

Reaction Conditions:

Stage #1: 2-chloro-3-fluoropyridinewith tert.-butyl lithium in tetrahydrofuran;n-heptane at -78; for 1.25 h;Inert atmosphere;
Stage #2: N-formyl-N,N',N'-trimethylethylenediaminewith n-butyllithium in tetrahydrofuran;hexane;n-heptane at -78 - -30; for 3 h;Inert atmosphere;Bouveault Aldehyde Synthesis;
Stage #3: allyl bromide

References:

Velcicky, Juraj;Schlapbach, Achim;Heng, Richard;Revesz, Laszlo;Pflieger, Daniel;Blum, Ernst;Hawtin, Stuart;Huppertz, Christine;Feifel, Roland;Hersperger, Rene [ACS Medicinal Chemistry Letters,2018,vol. 9,# 4,p. 392 - 396] Location in patent:supporting information

17282-04-1 Synthesis
2-Chloro-3-fluoropyridine

17282-04-1
367 suppliers
$7.00/10g

1189-06-6 Synthesis
Formamide, N-[(dimethylamino)methyl]-N-methyl-

1189-06-6
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5-Allyl-2-chloro-3-fluoroisonicotinaldehyde

1236769-86-0
1 suppliers
inquiry