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Perfluoroglutaric acid when reacted with methyl magnesium iodide affords
2,6 diol 2,6 dimethyl hexafluoro pyranI in high yield and 4-one, 1,2,3
hexafluoro caproic II acid in low yield. The former material appears to exist
in a range-melting form (64-79°C) and a very labile form of melting point
96-98°C. The 2,6 diol 2,6 dimethyl hexafluoro pyranI yields a mono semi
carbazoneIII, and also a monoIV and a di 2:4 dinitro phenyl hydrazone. V
The mono 2:1l dinitrophenyl hydrazone appears to be cyclic. Reduction both
with lithium aluminium hydride and sodium borohydride yields 2,6 diol 3,4,5
hexafluoro n-heptane.VI There is evidence to suggest that reaction with
dried calcium sulphate gives 2 ene, 2 methyl 3,4,5 hexafluor 6 one cyclo-hexaneVII
Reaction with benzoyl chloride affords 2,6 dibenzoate, 2,6
dimethyl hexafluoro pyran.VIII
4 one 1,2,3, hexafluorocaproic acid was characterised as a 2:4 dinitro
phenyl hydrazoneIX and also as an S benzyl thio-uranium salt.X Infra-red
spectral evidence suggests the S benzyl thio uranium salt probably exists in
the straight chain form.
Numbers in the above text refer to the Flow Sheet, Figure 1. |
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