Studies of 2-Ethylhexyl Acrylate. II
2-Ethylhexyl acrylate was synthesized through direct esterification of acrylic acid (1) with 2-ethylhexyl alcohol (2), and through ester-interchange reaction between methyl acrylate (3) and (2). The high-boiling by-products were found to be 2-ethylhexyl β-(2-ethylhexyloxy)propionate (4) in the forme...
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Veröffentlicht in: | Journal of Synthetic Organic Chemistry, Japan Japan, 1968/03/01, Vol.26(3), pp.258-263 |
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creator | YONEZAWA, Masaji SUZUKI, Shigenari ITO, Hiro SHODA, Hichiro |
description | 2-Ethylhexyl acrylate was synthesized through direct esterification of acrylic acid (1) with 2-ethylhexyl alcohol (2), and through ester-interchange reaction between methyl acrylate (3) and (2). The high-boiling by-products were found to be 2-ethylhexyl β-(2-ethylhexyloxy)propionate (4) in the former case ; and (4), methyl β-(2-ethylhexyloxy)propionate (5), 2-ethylhexyl methoxypropionate (6), and methyl β-methoxy. propionate (7) in the latter case. Apparent activation energies were calculated to be 18.1 kcal/mol for the esterification and 13.9 kcal/mol for the ester-interchange. On the other hand, the values for the formations of (4), (5) and (6) were about 27.1, 13.4 and 14.3 kcal/mol, respectively. The activation energy for (7) formation could not be measured due to its extremely low reaction velocity. In the synthesis of 2-ethylhexyl acrylate by direct esterification, it is recommended to add sulfuric acid, a catalyst, at a level of 1 mol % and phenol, a polymerization inhibitor, at a level of 0.1 wt % of the (1) used. For ester-interchange reaction, the use of sulfuric acid, a catalyst, at a level of 1 mol % of the (2) used and sulfur, a polymerization inhibitor, at a level of 0.1 wt % of the (3) used is recommended. Those reactions are conducted at temperatures below 110°C to effect an approximately 95% yield. |
doi_str_mv | 10.5059/yukigoseikyokaishi.26.258 |
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II</title><source>EZB-FREE-00999 freely available EZB journals</source><creator>YONEZAWA, Masaji ; SUZUKI, Shigenari ; ITO, Hiro ; SHODA, Hichiro</creator><creatorcontrib>YONEZAWA, Masaji ; SUZUKI, Shigenari ; ITO, Hiro ; SHODA, Hichiro</creatorcontrib><description>2-Ethylhexyl acrylate was synthesized through direct esterification of acrylic acid (1) with 2-ethylhexyl alcohol (2), and through ester-interchange reaction between methyl acrylate (3) and (2). The high-boiling by-products were found to be 2-ethylhexyl β-(2-ethylhexyloxy)propionate (4) in the former case ; and (4), methyl β-(2-ethylhexyloxy)propionate (5), 2-ethylhexyl methoxypropionate (6), and methyl β-methoxy. propionate (7) in the latter case. Apparent activation energies were calculated to be 18.1 kcal/mol for the esterification and 13.9 kcal/mol for the ester-interchange. On the other hand, the values for the formations of (4), (5) and (6) were about 27.1, 13.4 and 14.3 kcal/mol, respectively. The activation energy for (7) formation could not be measured due to its extremely low reaction velocity. In the synthesis of 2-ethylhexyl acrylate by direct esterification, it is recommended to add sulfuric acid, a catalyst, at a level of 1 mol % and phenol, a polymerization inhibitor, at a level of 0.1 wt % of the (1) used. For ester-interchange reaction, the use of sulfuric acid, a catalyst, at a level of 1 mol % of the (2) used and sulfur, a polymerization inhibitor, at a level of 0.1 wt % of the (3) used is recommended. Those reactions are conducted at temperatures below 110°C to effect an approximately 95% yield.</description><identifier>ISSN: 0037-9980</identifier><identifier>EISSN: 1883-6526</identifier><identifier>DOI: 10.5059/yukigoseikyokaishi.26.258</identifier><language>eng</language><publisher>The Society of Synthetic Organic Chemistry, Japan</publisher><ispartof>Journal of Synthetic Organic Chemistry, Japan, 1968/03/01, Vol.26(3), pp.258-263</ispartof><rights>The Society of Syhthetic Organic Chemistry, Japan</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids></links><search><creatorcontrib>YONEZAWA, Masaji</creatorcontrib><creatorcontrib>SUZUKI, Shigenari</creatorcontrib><creatorcontrib>ITO, Hiro</creatorcontrib><creatorcontrib>SHODA, Hichiro</creatorcontrib><title>Studies of 2-Ethylhexyl Acrylate. II</title><title>Journal of Synthetic Organic Chemistry, Japan</title><addtitle>J. Synth. Org. Chem. Jpn.</addtitle><description>2-Ethylhexyl acrylate was synthesized through direct esterification of acrylic acid (1) with 2-ethylhexyl alcohol (2), and through ester-interchange reaction between methyl acrylate (3) and (2). The high-boiling by-products were found to be 2-ethylhexyl β-(2-ethylhexyloxy)propionate (4) in the former case ; and (4), methyl β-(2-ethylhexyloxy)propionate (5), 2-ethylhexyl methoxypropionate (6), and methyl β-methoxy. propionate (7) in the latter case. Apparent activation energies were calculated to be 18.1 kcal/mol for the esterification and 13.9 kcal/mol for the ester-interchange. On the other hand, the values for the formations of (4), (5) and (6) were about 27.1, 13.4 and 14.3 kcal/mol, respectively. The activation energy for (7) formation could not be measured due to its extremely low reaction velocity. In the synthesis of 2-ethylhexyl acrylate by direct esterification, it is recommended to add sulfuric acid, a catalyst, at a level of 1 mol % and phenol, a polymerization inhibitor, at a level of 0.1 wt % of the (1) used. For ester-interchange reaction, the use of sulfuric acid, a catalyst, at a level of 1 mol % of the (2) used and sulfur, a polymerization inhibitor, at a level of 0.1 wt % of the (3) used is recommended. 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II</title><author>YONEZAWA, Masaji ; SUZUKI, Shigenari ; ITO, Hiro ; SHODA, Hichiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3038-4e733ccc36e12b6a9d9be232326720b62423ec73ea9d80027768a3f8819d3dcd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1968</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>YONEZAWA, Masaji</creatorcontrib><creatorcontrib>SUZUKI, Shigenari</creatorcontrib><creatorcontrib>ITO, Hiro</creatorcontrib><creatorcontrib>SHODA, Hichiro</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of Synthetic Organic Chemistry, Japan</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>YONEZAWA, Masaji</au><au>SUZUKI, Shigenari</au><au>ITO, Hiro</au><au>SHODA, Hichiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies of 2-Ethylhexyl Acrylate. II</atitle><jtitle>Journal of Synthetic Organic Chemistry, Japan</jtitle><addtitle>J. Synth. Org. Chem. Jpn.</addtitle><date>1968</date><risdate>1968</risdate><volume>26</volume><issue>3</issue><spage>258</spage><epage>263</epage><pages>258-263</pages><issn>0037-9980</issn><eissn>1883-6526</eissn><abstract>2-Ethylhexyl acrylate was synthesized through direct esterification of acrylic acid (1) with 2-ethylhexyl alcohol (2), and through ester-interchange reaction between methyl acrylate (3) and (2). The high-boiling by-products were found to be 2-ethylhexyl β-(2-ethylhexyloxy)propionate (4) in the former case ; and (4), methyl β-(2-ethylhexyloxy)propionate (5), 2-ethylhexyl methoxypropionate (6), and methyl β-methoxy. propionate (7) in the latter case. Apparent activation energies were calculated to be 18.1 kcal/mol for the esterification and 13.9 kcal/mol for the ester-interchange. On the other hand, the values for the formations of (4), (5) and (6) were about 27.1, 13.4 and 14.3 kcal/mol, respectively. The activation energy for (7) formation could not be measured due to its extremely low reaction velocity. In the synthesis of 2-ethylhexyl acrylate by direct esterification, it is recommended to add sulfuric acid, a catalyst, at a level of 1 mol % and phenol, a polymerization inhibitor, at a level of 0.1 wt % of the (1) used. For ester-interchange reaction, the use of sulfuric acid, a catalyst, at a level of 1 mol % of the (2) used and sulfur, a polymerization inhibitor, at a level of 0.1 wt % of the (3) used is recommended. Those reactions are conducted at temperatures below 110°C to effect an approximately 95% yield.</abstract><pub>The Society of Synthetic Organic Chemistry, Japan</pub><doi>10.5059/yukigoseikyokaishi.26.258</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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title | Studies of 2-Ethylhexyl Acrylate. II |
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