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.