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Study on Synthesis and NMR Characterization of 2,3-O-Hydroxyethyl Cellulose Depending on Synthesis Conditions
The synthesis of hydroxyethyl celluloses with regioselective functionalization in position 2 and 3 starting from triphenylmethyl (trityl) cellulose is described. The effects of reaction conditions upon both the degree of substitution and the distribution of the hydroxyethyl moieties were investigate...
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Published in: | Macromolecular symposia. 2010-08, Vol.294 (2), p.133-140 |
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container_title | Macromolecular symposia. |
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creator | Petzold-Welcke, Katrin Kötteritzsch, Manuela Fenn, Dominik Koschella, Andreas Heinze, Thomas |
description | The synthesis of hydroxyethyl celluloses with regioselective functionalization in position 2 and 3 starting from triphenylmethyl (trityl) cellulose is described. The effects of reaction conditions upon both the degree of substitution and the distribution of the hydroxyethyl moieties were investigated in detail. The interest was not only focused on regioselective functionalization within the anhydroglucose unit but also on the formation of oxyethylene side chains. To avoid the formation of oxyethylene side chains, 2-(2-bromoethoxy)tetrahydropyran was used as etherifying agent in comparison with 2-bromoethanol. By acidic hydrolysis, both protecting groups - trityl at 6 position and tetrahydropyran at the hydroxyethyl substituent - can be simultaneously cleaved off. The hydroxyethyl celluloses were characterized by one- and two-dimensional NMR spectroscopy in order to determine the substitution pattern. |
doi_str_mv | 10.1002/masy.201000003 |
format | article |
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The effects of reaction conditions upon both the degree of substitution and the distribution of the hydroxyethyl moieties were investigated in detail. The interest was not only focused on regioselective functionalization within the anhydroglucose unit but also on the formation of oxyethylene side chains. To avoid the formation of oxyethylene side chains, 2-(2-bromoethoxy)tetrahydropyran was used as etherifying agent in comparison with 2-bromoethanol. By acidic hydrolysis, both protecting groups - trityl at 6 position and tetrahydropyran at the hydroxyethyl substituent - can be simultaneously cleaved off. 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Symp</addtitle><description>The synthesis of hydroxyethyl celluloses with regioselective functionalization in position 2 and 3 starting from triphenylmethyl (trityl) cellulose is described. The effects of reaction conditions upon both the degree of substitution and the distribution of the hydroxyethyl moieties were investigated in detail. The interest was not only focused on regioselective functionalization within the anhydroglucose unit but also on the formation of oxyethylene side chains. To avoid the formation of oxyethylene side chains, 2-(2-bromoethoxy)tetrahydropyran was used as etherifying agent in comparison with 2-bromoethanol. By acidic hydrolysis, both protecting groups - trityl at 6 position and tetrahydropyran at the hydroxyethyl substituent - can be simultaneously cleaved off. The hydroxyethyl celluloses were characterized by one- and two-dimensional NMR spectroscopy in order to determine the substitution pattern.</description><subject>Cellulose</subject><subject>Hydrolysis</subject><subject>Hydroxyethyl celluloses</subject><subject>hydroxyethylation</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>protecting group</subject><subject>regioselective functionalization</subject><subject>Synthesis</subject><subject>Two dimensional</subject><issn>1022-1360</issn><issn>1521-3900</issn><issn>1521-3900</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkDtPwzAURiMEEuWxspKNhRQ_kjgeS3gUqQXRFlEmy9hOa0jjYqei4dfjKqiCibvcK-ucT9YXBCcQdCEA6GLBXdNFwN9-8E7QgQmCEaYA7PobIBRBnIL94MC5N09QSmAnWIzrlWxCU4XjpqrnymkX8kqG98NRmM-55aJWVn_xWnvEFCE6x9FD1G-kNetG1fOmDHNVlqvSOBVeqaWqpK5mf_Ny4x83Ae4o2Ct46dTxzz4MJjfXk7wfDR5u7_LeIBI4wzgqBJFZnAoIKMGxwFK9Eg6RiLOUFhAnCIhUxplIKCEEU4EgFpQXNEMgk7HEh8FZG7u05mOlXM0W2gn_TV4ps3KMApgSAEnsyW5LCmucs6pgS6sX3DYMArZplW1aZdtWvUBb4VOXqvmHZsPe-OW3G7WudrVab11u31lKMEnY8_0t6z-Okst0CtjU86ctX3DD-Mxqx57GPg4DmGUJSRD-BsGUlDc</recordid><startdate>201008</startdate><enddate>201008</enddate><creator>Petzold-Welcke, Katrin</creator><creator>Kötteritzsch, Manuela</creator><creator>Fenn, Dominik</creator><creator>Koschella, Andreas</creator><creator>Heinze, Thomas</creator><general>Wiley-VCH Verlag</general><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>FBQ</scope><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>201008</creationdate><title>Study on Synthesis and NMR Characterization of 2,3-O-Hydroxyethyl Cellulose Depending on Synthesis Conditions</title><author>Petzold-Welcke, Katrin ; Kötteritzsch, Manuela ; Fenn, Dominik ; Koschella, Andreas ; Heinze, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3833-fc7d846c109734c3deb7a12c4869f13520c6d48c5977739c213c9af98208d4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Cellulose</topic><topic>Hydrolysis</topic><topic>Hydroxyethyl celluloses</topic><topic>hydroxyethylation</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>protecting group</topic><topic>regioselective functionalization</topic><topic>Synthesis</topic><topic>Two dimensional</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Petzold-Welcke, Katrin</creatorcontrib><creatorcontrib>Kötteritzsch, Manuela</creatorcontrib><creatorcontrib>Fenn, Dominik</creatorcontrib><creatorcontrib>Koschella, Andreas</creatorcontrib><creatorcontrib>Heinze, Thomas</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Macromolecular symposia.</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Petzold-Welcke, Katrin</au><au>Kötteritzsch, Manuela</au><au>Fenn, Dominik</au><au>Koschella, Andreas</au><au>Heinze, Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study on Synthesis and NMR Characterization of 2,3-O-Hydroxyethyl Cellulose Depending on Synthesis Conditions</atitle><jtitle>Macromolecular symposia.</jtitle><addtitle>Macromol. Symp</addtitle><date>2010-08</date><risdate>2010</risdate><volume>294</volume><issue>2</issue><spage>133</spage><epage>140</epage><pages>133-140</pages><issn>1022-1360</issn><issn>1521-3900</issn><eissn>1521-3900</eissn><abstract>The synthesis of hydroxyethyl celluloses with regioselective functionalization in position 2 and 3 starting from triphenylmethyl (trityl) cellulose is described. The effects of reaction conditions upon both the degree of substitution and the distribution of the hydroxyethyl moieties were investigated in detail. The interest was not only focused on regioselective functionalization within the anhydroglucose unit but also on the formation of oxyethylene side chains. To avoid the formation of oxyethylene side chains, 2-(2-bromoethoxy)tetrahydropyran was used as etherifying agent in comparison with 2-bromoethanol. 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subjects | Cellulose Hydrolysis Hydroxyethyl celluloses hydroxyethylation NMR NMR spectroscopy Nuclear magnetic resonance protecting group regioselective functionalization Synthesis Two dimensional |
title | Study on Synthesis and NMR Characterization of 2,3-O-Hydroxyethyl Cellulose Depending on Synthesis Conditions |
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