Process for the preparation of azolylether ketones
The application relates to a process for the preparation of azolylether ketones of the general formula I, in which R represents chlorine, bromine, phenyl, alkyl having from 1 to 3 carbon atoms or nitro, R represents alkyl having from 1 to 4 carbon atoms, phenyl or phenyl substituted by chlorine, A r...
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Main Authors | , , , , , , , , , , , |
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Format | Patent |
Language | English German |
Published |
15.12.1988
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Edition | 4 |
Subjects | |
Online Access | Get full text |
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Abstract | The application relates to a process for the preparation of azolylether ketones of the general formula I, in which R represents chlorine, bromine, phenyl, alkyl having from 1 to 3 carbon atoms or nitro, R represents alkyl having from 1 to 4 carbon atoms, phenyl or phenyl substituted by chlorine, A represents the grouping = CH- or represents a nitrogen atom, and n represents 0, 1, 2 or 3, where ether ketones of the general formula IV, in which R , R and n have the abovementioned meanings, are reacted, at a temperature of 80-140@C, with equimolar quantities, or at most with a 25 mol% excess, of a halogenating agent, preferably sulphuryl chloride, the haloether ketones, obtained in this way or by any other method, of the general formula II, in which R , R and n have the abovementioned meanings, and X represents chlorine or bromine, are reacted with azoles of the general formula III, in which A has the abovementioned meaning, in a molar ratio of 1:2 at a temperature of 100-180@C, and the azolylether ketones are isolated from the reaction mixture by washing with water or with organic solvents, or by separation. |
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AbstractList | The application relates to a process for the preparation of azolylether ketones of the general formula I, in which R represents chlorine, bromine, phenyl, alkyl having from 1 to 3 carbon atoms or nitro, R represents alkyl having from 1 to 4 carbon atoms, phenyl or phenyl substituted by chlorine, A represents the grouping = CH- or represents a nitrogen atom, and n represents 0, 1, 2 or 3, where ether ketones of the general formula IV, in which R , R and n have the abovementioned meanings, are reacted, at a temperature of 80-140@C, with equimolar quantities, or at most with a 25 mol% excess, of a halogenating agent, preferably sulphuryl chloride, the haloether ketones, obtained in this way or by any other method, of the general formula II, in which R , R and n have the abovementioned meanings, and X represents chlorine or bromine, are reacted with azoles of the general formula III, in which A has the abovementioned meaning, in a molar ratio of 1:2 at a temperature of 100-180@C, and the azolylether ketones are isolated from the reaction mixture by washing with water or with organic solvents, or by separation. |
Author | BESAN, JANOS BAGI, LASZLO SZANTO, ANDRAS., BUDAPEST, HU SZALONTAI, GABOR PERNYESZI, JOZSEF., VESZPREM, HU TILINGER, FERENC, VESZPREM, HU KULCSAR, LASZLO SIMON, KATALIN SZABO, GEB. RAVASZ, BERNADETT SIMON, ZOLTAN GESZTELYI NAGY, GEB. BABOCZKY, JUDIT GESZTELYI NAGY, ADAM |
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DocumentTitleAlternate | VERFAHREN ZUR HERSTELLUNG VON AZOLYLETHERKETONEN |
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Notes | Application Number: DE19883817737 |
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Snippet | The application relates to a process for the preparation of azolylether ketones of the general formula I, in which R represents chlorine, bromine, phenyl,... |
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Title | Process for the preparation of azolylether ketones |
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