Direct fluorination of gamma-butyrolactone

Citation
Y. Sasaki et al., Direct fluorination of gamma-butyrolactone, J FLUORINE, 108(1), 2001, pp. 117-120
Citations number
18
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF FLUORINE CHEMISTRY
ISSN journal
00221139 → ACNP
Volume
108
Issue
1
Year of publication
2001
Pages
117 - 120
Database
ISI
SICI code
0022-1139(200103)108:1<117:DFOG>2.0.ZU;2-C
Abstract
gamma -Butyrolactone was fluorinated by molecular fluorine to obtain its mo no-fluorinated derivatives for possible lithium battery electrolyte applica tion. The reaction was carried out at 30 degreesC by introducing 20% F-2/N- 2 gas into gamma -butyrolactone without solvent. Major products were beta - fluoro-gamma -butyrolactone and gamma -fluoro-gamma -butyrolactone, which c annot be obtained by conventional organic synthesis. Selectivity to gamma - isomer was enhanced by the addition of NaF as a HF scavenger. (C) 2001 Else vier Science B.V. All rights reserved.