Apr 2010 to Dec 2010 Performance AnalystJPMorgan Chase Boston, MA Jun 2008 to Dec 2009 Fund AccountantMorgan Stanley Smith Barney Boston, MA Aug 2007 to Dec 2007 Private Wealth Intern
Education:
Simmons College Boston, MA May 2008 Bachelor of Arts in Economics
Helen Ngo - North Wales PA, US Thomas A. Foglia - Lafayette Hill PA, US
Assignee:
The United States of America as represented by the Secretary of Agriculture - Washington DC
International Classification:
C07C 57/02 C07C 55/00
US Classification:
562595, 562590
Abstract:
A method of producing dicarboxylic acids (e. g. , α,ω dicarboxylic acids) by reacting a compound having a terminal COOH (e. g. , unsaturated fatty acid such as oleic acid) and containing at least one carbon-carbon double bond with a second generation Grubbs catalyst in the absence of solvent to produce dicarboxylic acids. The method is conducted in an inert atmosphere (e. g. , argon, nitrogen). The process also works well with mixed unsaturated fatty acids obtained from soybean, rapeseed, tall, and linseed oils.
Process For Preparing Saturated Branched Chain Fatty Acids
Helen Ngo - North Wales PA, US Thomas A. Foglia - Lafayette Hill PA, US
International Classification:
C07C 51/353
US Classification:
554154
Abstract:
A process for preparing saturated branched chain fatty acids or alkyl esters thereof involving subjecting unsaturated fatty acids having 10 to 25 carbon atoms, alkyl esters thereof or mixtures thereof to a skeletal isomerization reaction in the presence of water or a lower alcohol at a temperature of about 240 C. to about 280 C. using a combination of a stericly hindered Lewis base and zeolite as a Brönsted or Lewis acid catalyst, and isolating saturated branched chain fatty acids or alkyl esters thereof or mixtures thereof from the reaction mixture obtained by the skeletal isomerization reaction. The yield of said saturated branched chain fatty acids is ≧70 wt %. The stericly hindered Lewis base is a tertiary amine or phosphine with linear or branched C1 to C6 alkyl or phenyl groups attached thereto.
Process For Preparing Saturated Branched Chain Fatty Acids
Helen Ngo - North Wales PA, US Thomas A. Foglia - Lafeyette Hill PA, US
International Classification:
C07C 67/48
US Classification:
554142
Abstract:
A process for preparing saturated branched chain fatty acids or alkyl esters thereof involving subjecting unsaturated fatty acids having 10 to 25 carbon atoms, alkyl esters thereof or mixtures thereof to a skeletal isomerization reaction in the presence of water or a lower alcohol at a temperature of about 240 C. to about 280 C. using a combination of a stericly hindered Lewis base and zeolite as a Brönsted or Lewis acid catalyst, and isolating saturated branched chain fatty acids or alkyl esters thereof or mixtures thereof from the reaction mixture obtained by the skeletal-isomerization reaction. The yield of said saturated branched chain fatty acids is ≧70 wt %. The stericly hindered Lewis base is a tertiary amine or phosphine with linear or branched C1 to C6 alkyl or phenyl groups attached thereto.