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research article

Silyl-mediated halogen/halogen displacement in pyridines and other heterocycles

Schlosser, Manfred  
•
Cottet, Fabrice  
2002
European Journal of Organic Chemistry

Heating with bromotrimethylsilane converts 2-chloropyridine into 2-bromopyridine and 2-chloro-6-methylpyridine into 2-bromo-6-methylpyridine. Both 2-chloropyridines and 2-bromopyridines give the corresponding iodo compd. when treated with in situ generated iodotrimethylsilane. Although 3- and 4-chloropyridine are completely inert, 2,4-dichloropyridine undergoes the halogen/halogen exchange simultaneously at the 2- and 4-position. Halogen displacement takes place exclusively at the 2-position with 2,3-dichloropyridine and 2,5-dichloropyridine. In agreement with the intermediacy of N-trimethylsilylpyridinium salts as a prerequisite for the occurrence of halogen exchange, neither 2-fluoropyridine and 2-fluoro-6-methylpyridine nor any 2,6-dihalopyridine reacts. Finally, bromine/chlorine and iodine/chlorine substitution can also be accomplished with 2- or 4-chloroquinoline, 1-chloroisoquinoline, 2-chloropyrimidine, chloropyrazine, and 2,3-dichloroquinoxaline as substrates. [on SciFinder (R)]

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Type
research article
DOI
10.1002/1099-0690(200212)2002:24<4181::AID-EJOC4181>3.0.CO;2-M
Web of Science ID

WOS:000180032700011

Author(s)
Schlosser, Manfred  
•
Cottet, Fabrice  
Date Issued

2002

Published in
European Journal of Organic Chemistry
Issue

24

Start page

4181

End page

4184

Subjects

Exchange reaction (silyl-mediated halogen/halogen exchange reactions of pyridines and other heterocycles)

•

silyl mediated halogen halogen displacement pyridine; exchange halogen silyl mediated pyridine

Note

CAN 138:321108 27-16 Heterocyclic Compounds (One Hetero Atom) Institut de Chimie moleculaire et biologique,Ecole Polytechnique Federale,Lausanne,Switz. Journal 1434-193X written in English. 86-98-6 (4,7-Dichloroquinoline); 109-09-1 (2-Chloropyridine); 612-62-4 (2-Chloroquinoline); 1722-12-9 (2-Chloropyrimidine); 2213-63-0; 2402-77-9 (2,3-Dichloropyridine); 2857-97-8 (Bromotrimethylsilane); 14508-49-7 (Chloropyrazine); 16029-98-4 (Iodotrimethylsilane); 16110-09-1 (2,5-Dichloropyridine); 18368-63-3 (2-Chloro-6-methylpyridine); 19493-44-8 (1-Chloroisoquinoline); 26452-80-2 (2,4-Dichloropyridine) Role: RCT (Reactant), RACT (Reactant or reagent) (silyl-mediated halogen/halogen exchange reactions of pyridines and other heterocycles); 109-04-6P (2-Bromopyridine); 5315-25-3P (2-Bromo-6-methylpyridine) Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (silyl-mediated halogen/halogen exchange reactions of pyridines and other heterocycles); 624-28-2P (2,5-Dibromopyridine); 1532-71-4P (1-Bromoisoquinoline); 2005-43-8P (2-Bromoquinoline); 4595-60-2P (2-Bromopyrimidine); 5029-67-4P (2-Iodopyridine); 6560-83-4P (2-Iodoquinoline); 19658-77-6P (1-Iodoisoquinoline); 23719-78-0P (2,3-Dibromoquinoxaline); 56423-63-3P (Bromopyrazine); 58530-53-3P (2,4-Dibromopyridine); 62674-71-9P (2-Iodo-6-methylpyridine); 77332-89-9P (2-Iodo-3-chloropyridine); 96424-68-9P (2-Bromo-3-chloropyridine); 98519-65-4P; 244221-57-6P Role: SPN (Synthetic preparation), PREP (Preparation) (silyl-mediated halogen/halogen exchange reactions of pyridines and other heterocycles)

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSCO  
Available on Infoscience
March 3, 2006
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/226989
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