A useful conversion of alcohols to alkyl fluorides
β Scribed by David A Flosser; Roy A Olofson
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 113 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A useful conversion of alcohols to alkyl fluorides via their fluoroformates is introduced. The fluoroformates are obtained in nearly quantitative yield from the alcohols by treatment with COF 2 (generated in situ from bis(trichloromethyl) carbonate) in ether with KF as an added acid scavenger. The neat fluoroformates are cleaved to the fluorides by heating at 120-125Β°C using hexabutylguanidinium fluoride (HBGF) as the catalyst.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
Caesium fluoroxysulphate in acetonitrile medium at 39C converts primary alcohols and alkyl, as well as aryl aldehydes, to acid fluorides in high yield.