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		    <title>PatentStorm -> Patents -> Organic compounds -- part of the class 532-570 series</title>
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		    <description>Recent patents filings in USPTO Class 558 Organic compounds -- part of the class 532-570 series.</description>
		    <pubDate>Tue, 7 Feb 2012 16:02:58</pubDate>
		    <managingEditor>patents@patentstorm.us</managingEditor>
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			         <title><![CDATA[Process for producing diphenyl carbonate]]></title>
			         <link>http://www.patentstorm.us/patents/8110698/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8110698</li><li><strong>Publication Date:</strong> &nbsp;2012-02-07</li><li><strong>Inventor:</strong> &nbsp;Ryu, J. Yong</li></ul>
<p>Processes for producing diaryl carbonates are disclosed, where such processes may provide for the production of diaryl carbonates from green house gases, such as carbon dioxide. The processes disclosed advantageously integrate diethyl carbonate and diaryl carbonate production, eliminating the need for solvent-based extractive distillation, as is commonly required when producing diaryl carbonates from dimethyl carbonate, providing for the integration of separation equipment and raw material ...<br /> 		
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			         <title><![CDATA[Succinic acid diester derivative, process for production thereof, and use of the derivative in the production of pharmaceutical preparation]]></title>
			         <link>http://www.patentstorm.us/patents/8106230/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8106230</li><li><strong>Publication Date:</strong> &nbsp;2012-01-31</li><li><strong>Inventors:</strong> &nbsp;Inagaki, Takashi; Yamakawa, Yoshikazu</li></ul>
<p>The present invention provides with a process of preparing an optically active succinimide derivative, which is a key intermediate for production of ranirestat. A compound (3) is easily prepared by treating the derivative of succinic acid diester of the formula (2):</p>
<p><chemistry>

</chemistry>
<br></br>
wherein R<sup>1 </sup>is an amino group protected with a group removed by hydrogenolysis or a tert-butoxycarbonylamino group and R<sup>2 </sup>is an ethyl group optionally substituted ...<br /> 		
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			         <title><![CDATA[Process for improving adiponitrile quality]]></title>
			         <link>http://www.patentstorm.us/patents/8101790/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8101790</li><li><strong>Publication Date:</strong> &nbsp;2012-01-24</li><li><strong>Inventors:</strong> &nbsp;Murphree, Bruce E.; Ostermaier, John J.</li></ul>
<p>A process and apparatus for reacting deleterious impurities contained in adiponitrile (ADN) comprises feeding ADN and an ozone containing gas into a co-current plug flow reactor containing static mixer elements, to oxidize at least a portion of the impurities, thereby producing a reactor discharge, which is processed to produce an ozone-treated ADN ...<br /> 		
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			         <title><![CDATA[Isothermal process for phosphoromonochloridite synthesis]]></title>
			         <link>http://www.patentstorm.us/patents/8097749/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8097749</li><li><strong>Publication Date:</strong> &nbsp;2012-01-17</li><li><strong>Inventor:</strong> &nbsp;Miller, Glenn A.</li></ul>
<p>The present invention relates to a process for preparation of a phosphoromonochloridite in high yield by contacting phosphorus trichloride (PCl<sub>3</sub>) with an aromatic diol in a solution of one or more organic solvents under reaction conditions sufficient to produce the phosphoromonochloridite. The reaction is carried out by adding a feed solution containing the aromatic diol dissolved in a first organic solvent into a reaction zone containing PCl<sub>3</sub>, and optionally one or ...<br /> 		
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			         <title><![CDATA[Amorphous compound and production method thereof]]></title>
			         <link>http://www.patentstorm.us/patents/8097748/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8097748</li><li><strong>Publication Date:</strong> &nbsp;2012-01-17</li><li><strong>Inventors:</strong> &nbsp;Awa, Hideaki; Kimura, Kenji; Kitamura, Kazuhiro</li></ul>
<p>An amorphous compound of the formula (1):</p>
<p><chemistry>

</chemistry>
</p>
<p>wherein the temperature showing an endothermic peak by differential scanning calorimetry (DSC) is 40 to 80° C. and the solution rate into n-hexane at 25° C. in the following test system is 1.5 mg/sec or more.</p>
<p><Test System Regarding Solution Rate></p>
<p>At 25° C., 1 g of a specimen is charged into a vessel containing 50 g of n-hexane (capacity: 100 ml, outer diameter: 55 mm, height: 70 mm), a 38 mm ...<br /> 		
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			         <title><![CDATA[Process for the alkylation of phosphorus-containing compounds]]></title>
			         <link>http://www.patentstorm.us/patents/8097747/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8097747</li><li><strong>Publication Date:</strong> &nbsp;2012-01-17</li><li><strong>Inventors:</strong> &nbsp;Yao, Qiang; Levchik, Sergi V.</li></ul>
<p>A process for alkylating a phosphorus-containing compound to provide an alkylated phosphorus-containing compound is provided which comprises alkylating 5 phosphorus-containing compound possessing at least one phosphorus-hydrogen alkylatable site with reactant which generates alkene and/or cycloalkene alkylating agent in situ in the presence of initiator, the alkylene and/or cycloalkylene alkylating agent alkylating the phosphorus-containing component to provide alkylated ...<br /> 		
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			         <title><![CDATA[Method for producing 2-isopropenyl-5-methyl-4-hexen-1-yl 3-methyl-2-butenoate]]></title>
			         <link>http://www.patentstorm.us/patents/8097746/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8097746</li><li><strong>Publication Date:</strong> &nbsp;2012-01-17</li><li><strong>Inventors:</strong> &nbsp;Ujita, Katsuji; Sato, Junko; Fukumoto, Takashi</li></ul>
<p>The present invention provides a method of producing 2-isopropenyl-5-methyl-4-hexen-1-yl 3-methyl-2-butenoate industrially advantageously in a high yield. More particularly, the present invention provides a method of producing 2-isopropenyl-5-methyl-4-hexen-1-yl 3-methyl-2-butenoate represented by the following formula (IV):</p>
<p><chemistry>

</chemistry>
<br></br>
which comprises reacting 2-isopropenyl-5-methyl-4-hexen-1-ol with an organic sulfonyl halide in the presence of a basic ...<br /> 		
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