Catalytic fluorination of trichloroethene by anhydrous hydrogen fluoride in the presence of fluorinated chromia under static conditions. Synthesis of[F-18]-labelled CF3CH2F and [Cl-36]-labelled CF3CH2Cl. Catalytic dehydrofluorination of CF3CH2F and CF3CH2Cl

Citation
Aw. Baker et al., Catalytic fluorination of trichloroethene by anhydrous hydrogen fluoride in the presence of fluorinated chromia under static conditions. Synthesis of[F-18]-labelled CF3CH2F and [Cl-36]-labelled CF3CH2Cl. Catalytic dehydrofluorination of CF3CH2F and CF3CH2Cl, J FLUORINE, 102(1-2), 2000, pp. 279-284
Citations number
32
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF FLUORINE CHEMISTRY
ISSN journal
00221139 → ACNP
Volume
102
Issue
1-2
Year of publication
2000
Pages
279 - 284
Database
ISI
SICI code
0022-1139(200003)102:1-2<279:CFOTBA>2.0.ZU;2-V
Abstract
Catalytic fluorination of trichloroethene by anhydrous hydrogen fluoride at 653 K in the presence of fluorinated amorphous chromia under static condit ions leads to a mixture of products in which partially halogenated olefins predominate. These are converted to mixtures containing CF3CH2F and CF3CH2C l by a second fluorination using fresh catalyst. The results of product ana lyses from reactions carried out under various conditions have been used to design a synthesis of [F-18]-CF3CH2F from CCl2=CHCl. It is proposed that [ F-18] labelling occurs via direct [F-18]- for [F-19] exchange rather than b y a dehydrofluorination/hydrofluorination route. [Cl-36]-labelled CF3CH2Cl is readily prepared from CF3CH2F and (HCl)-Cl-36 in the presence of chromia catalysts. Enthalpies of dehydrofluorination of CF3CH2F and CF3CH2Cl in th e vapour phase have been computed.(1) (C) 2000 Elsevier Science S.A. All ri ghts reserved.