Back to Search
Start Over
Flow Giese reaction using cyanoborohydride as a radical mediator
- Source :
- Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1791-1796 (2013), Beilstein Journal of Organic Chemistry
- Publication Year :
- 2013
- Publisher :
- Beilstein-Institut, 2013.
-
Abstract
- Tin-free Giese reactions, employing primary, secondary, and tertiary alkyl iodides as radical precursors, ethyl acrylate as a radical trap, and sodium cyanoborohydride as a radical mediator, were examined in a continuous flow system. With the use of an automated flow microreactor, flow reaction conditions for the Giese reaction were quickly optimized, and it was found that a reaction temperature of 70 °C in combination with a residence time of 10–15 minutes gave good yields of the desired addition products.
- Subjects :
- Letter
flow chemistry
microreactor
lcsh:QD241-441
chemistry.chemical_compound
Reaction temperature
iodoalkanes
lcsh:Organic chemistry
Polymer chemistry
Organic chemistry
continuous flow system
lcsh:Science
Alkyl
Reaction conditions
chemistry.chemical_classification
Sodium cyanoborohydride
Continuous flow
Organic Chemistry
Flow chemistry
tin-free Giese reaction
Chemistry
chemistry
cyanoborohydride
Ethyl acrylate
lcsh:Q
Microreactor
Subjects
Details
- Language :
- English
- ISSN :
- 18605397
- Volume :
- 9
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Beilstein Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....23e4379c9b6a4c6f1672826bea709068