Verfahren zur Synthese von Acryl- und Methacrylverhindungen durch Eliminierungs- und Austauschreaktionen in flüssiger Phase

Synthesis of acryl- and methacryl derivatives via elimination and interchange reactions of suitable compounds are described. Decarboxylation of maleic monoesters in a pyridine base/basic copper salts pyrolysis bath at 210 °C leads to the corresponding acrylic ester in quantitative yields. Thus, i...

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Main Authors: E. Schindelmann-Pichler, O. Sylla-Trietsch, K. Hering, H. Zweifel, Th. Voelker
Format: Article
Language:deu
Published: Swiss Chemical Society 1973-02-01
Series:CHIMIA
Online Access:https://www.chimia.ch/chimia/article/view/9058
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author E. Schindelmann-Pichler
O. Sylla-Trietsch
K. Hering
K. Hering
H. Zweifel
Th. Voelker
author_facet E. Schindelmann-Pichler
O. Sylla-Trietsch
K. Hering
K. Hering
H. Zweifel
Th. Voelker
author_sort E. Schindelmann-Pichler
collection DOAJ
description Synthesis of acryl- and methacryl derivatives via elimination and interchange reactions of suitable compounds are described. Decarboxylation of maleic monoesters in a pyridine base/basic copper salts pyrolysis bath at 210 °C leads to the corresponding acrylic ester in quantitative yields. Thus, isopropyl- and isobutyl acrylates, which were previously prepared in relatively low yields via esterification of acrylic acid, can be synthethised in a single step. Since both the acrylates do not form azeotropic mixtures with most alcohols, special acrylates of higher alcohols can be obtained by transesterification. Synthesis of methacrylic acid or methyl methacrylate is carried out by dehydration of α-hydroxy isobutyric acid at 260°C in an organic, polar, inert and high boiling point solvent, employing catalytic quantities of sodium hydroxide. This is achieved by reacting the molten acid or in acetic or methanolic acid solution. The procedures described can be employed for continuous synthesis of acryl- and methacryl derivatives. Furthermore, these procedures do not contribute towards environmental pollution.
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id doaj-art-738855a10a7c4e18b3f4dd5500cf8b7e
institution Kabale University
issn 0009-4293
2673-2424
language deu
publishDate 1973-02-01
publisher Swiss Chemical Society
record_format Article
series CHIMIA
spelling doaj-art-738855a10a7c4e18b3f4dd5500cf8b7e2025-08-20T03:53:27ZdeuSwiss Chemical SocietyCHIMIA0009-42932673-24241973-02-0127210.2533/chimia.1973.59Verfahren zur Synthese von Acryl- und Methacrylverhindungen durch Eliminierungs- und Austauschreaktionen in flüssiger PhaseE. Schindelmann-Pichler0O. Sylla-Trietsch1K. Hering2K. Hering3H. Zweifel4Th. Voelker5Forschungslaboratorium der Lonza AG, Freiburg (Schweiz)Forschungslaboratorium der Lonza AG, Freiburg (Schweiz)Forschungslaboratorium der Lonza AG, Freiburg (Schweiz)Forschungslaboratorium der Lonza AG, Freiburg (Schweiz)Forschungslaboratorium der Lonza AG, Freiburg (Schweiz)Forschungslaboratorium der Lonza AG, Freiburg (Schweiz) Synthesis of acryl- and methacryl derivatives via elimination and interchange reactions of suitable compounds are described. Decarboxylation of maleic monoesters in a pyridine base/basic copper salts pyrolysis bath at 210 °C leads to the corresponding acrylic ester in quantitative yields. Thus, isopropyl- and isobutyl acrylates, which were previously prepared in relatively low yields via esterification of acrylic acid, can be synthethised in a single step. Since both the acrylates do not form azeotropic mixtures with most alcohols, special acrylates of higher alcohols can be obtained by transesterification. Synthesis of methacrylic acid or methyl methacrylate is carried out by dehydration of α-hydroxy isobutyric acid at 260°C in an organic, polar, inert and high boiling point solvent, employing catalytic quantities of sodium hydroxide. This is achieved by reacting the molten acid or in acetic or methanolic acid solution. The procedures described can be employed for continuous synthesis of acryl- and methacryl derivatives. Furthermore, these procedures do not contribute towards environmental pollution. https://www.chimia.ch/chimia/article/view/9058
spellingShingle E. Schindelmann-Pichler
O. Sylla-Trietsch
K. Hering
K. Hering
H. Zweifel
Th. Voelker
Verfahren zur Synthese von Acryl- und Methacrylverhindungen durch Eliminierungs- und Austauschreaktionen in flüssiger Phase
CHIMIA
title Verfahren zur Synthese von Acryl- und Methacrylverhindungen durch Eliminierungs- und Austauschreaktionen in flüssiger Phase
title_full Verfahren zur Synthese von Acryl- und Methacrylverhindungen durch Eliminierungs- und Austauschreaktionen in flüssiger Phase
title_fullStr Verfahren zur Synthese von Acryl- und Methacrylverhindungen durch Eliminierungs- und Austauschreaktionen in flüssiger Phase
title_full_unstemmed Verfahren zur Synthese von Acryl- und Methacrylverhindungen durch Eliminierungs- und Austauschreaktionen in flüssiger Phase
title_short Verfahren zur Synthese von Acryl- und Methacrylverhindungen durch Eliminierungs- und Austauschreaktionen in flüssiger Phase
title_sort verfahren zur synthese von acryl und methacrylverhindungen durch eliminierungs und austauschreaktionen in flussiger phase
url https://www.chimia.ch/chimia/article/view/9058
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