Volume 21, Issue 37
Heterocyclic Compounds
Full Access

ChemInform Abstract: Fluorinated Acetylenes. Part 7. Preparation and Some Reactions of 4,4,4-Trifluorobut-2-ynoic Acid and 1-Phenyl-4,4,4-trifluorobut-2-yn-1-ol.

S. TAJAMMAL

S. TAJAMMAL

Dep. Chem., Univ. Manchester Inst. Sci. Technol., Manchester M60 1QD, UK

Search for more papers by this author
A. E. TIPPING

A. E. TIPPING

Dep. Chem., Univ. Manchester Inst. Sci. Technol., Manchester M60 1QD, UK

Search for more papers by this author
First published: September 11, 1990

Abstract

Some reactions of the lithium salt (I) of 3,3,3-trifluoropropyne (prepared by bubbling the trifluoropropyne into a solution of n-butyllithium in hexane and dibutyl ether) with electrophiles such as the chloroformates (II), carbon dioxide (V), and benzaldehyde (VII) are reported.

ChemInform Abstract

Some reactions of the lithium salt (I) of 3,3,3-trifluoropropyne (prepared by bubbling the trifluoropropyne into a solution of n-butyllithium in hexane and dibutyl ether) with electrophiles such as the chloroformates (II), carbon dioxide (V), and benzaldehyde (VII) are reported. The expected products are obtained in moderate to good yields. 4,4,4-Trifluorobut-2-ynoic acid (VI) reacts with excess diazomethane (IX) to give the pyrazolines (XI) - (XIII) via the methyl ester (X).

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.