VERFAHREN ZUR HERSTELLUNG VOM ENOLLAKTON DER 2- OXYCYCLOHEXYLIDEN-ESSIGSÄURE UND VERWENDUNG ZUR HERSTELLUNG VOM 2-COUMARANON

Preparation of 2-oxo cyclohexylidene acetic acid enol-lactone (I) comprises: (i) reacting glyoxylic acid with cyclohexanone in the presence of a halogenated acid to give a crude reaction product; and (ii) dissolving the above product in an organic solvent in the presence of a strong soluble acid or...

Full description

Saved in:
Bibliographic Details
Main Authors PERRARD, ALAIN, CARMONA, LAURENT, VALLEJOS, JEAN-CLAUDE, CARMONA, NATHALIE
Format Patent
LanguageGerman
Published 15.06.2001
Edition7
Subjects
APPARATUS THEREFOR
CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY
CHEMISTRY
GENERAL METHODS OF ORGANIC CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
PERFORMING OPERATIONS
PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
THEIR RELEVANT APPARATUS
TRANSPORTING
Online AccessGet full text

Cover

More Information
Summary:Preparation of 2-oxo cyclohexylidene acetic acid enol-lactone (I) comprises: (i) reacting glyoxylic acid with cyclohexanone in the presence of a halogenated acid to give a crude reaction product; and (ii) dissolving the above product in an organic solvent in the presence of a strong soluble acid or a strongly acidic resin. In (i), the acid is preferably HCl added in a 1-100% molar amount w.r.t. glyoxylic acid and the reagents are heated above 50 degrees C. The resulting crude product is dissolved in a solvent containing a benzene ring and treated with methane sulphonic acid or p-toluene sulphonic acid or with a strongly acidic sulphonic Amberlist (RTM) resin.
Bibliography:Application Number: AT19970401561T