Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.703992
Title: Acylation by acetyl trifluoracetate and trifluoroacetic anhydride
Author: McNamara, Patricia Margaret
Awarding Body: University of London
Current Institution: Royal Holloway, University of London
Date of Award: 1967
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Abstract:
The reaction of acetic anhydride with trifluoroacetic anhydride in carbon tetrachloride has been studied kinetically and it was found that under anhydrous conditions no reaction occurred, but when small quantities of either acetic or trifluoroacetic acid were present there was conversion of the symmetric anhydrides to acetyltrifluoroacetate. The mechanism of this acid catalysis was discussed. The acylation of phenols in carbon tetrachloride by acetic anhydride, trifluoroacetic anhydride and acetyl trifluoroacetate was investigated in the presence and absence of pyridine. In the case of the symmetric anhydrides the presence of pyridine caused a considerable increase in the rate of the reaction and with acetyl trifluoroacetate there was a change from acetate to trifluoroacetate formation. Pyridine had little or no effect on the rate or product of the reaction of alcohols with any of the anhydrides. The mechanism of the effect of pyridine on the reactions between hydroxy compounds and the anhydrides mentioned above is discussed and an attempt to decide whether the catalysis is due to hydrogen bonding between the pyridine and the hydroxy compound or to reaction of the pyridine with the anhydride is made.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.703992  DOI: Not available
Keywords: Organic Chemistry
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