US EPA

1177825 

Journal Article 

Synthesis of chloroalkoxy eicosanoic and docosanoic acids from meadowfoam fatty acids by oxidation with aqueous sodium hypochlorite 

Mund, MS; Isbell, TA 

1999 

Yes 

Journal of the American Oil Chemists' Society
ISSN: 0003-021X
EISSN: 1558-9331 

American Oil Chemists' Soc 

Champaign 

76 

10 

1189-1200 

English 

10.1007/BF03028872 

WOS:000083216200014 

Chloroalkoxy substituted C20 and C22 fatty acids can be synthesized from the unsaturated fatty acids in meadow foam oil by reaction of the fatty acids with primary or secondary alcohols and an aqueous sodium hypochlorite solution (commercial bleach). The reactions are conducted at room temperature for 3 h. Chlorohydroxy fatty acid derivatives are formed as by-products owing to the presence of water in the reaction mixture. Chlorinated δ-lactones are also produced by direct reaction of sodium hypochlorite with the Δ5 unsaturated fatty acids present in meadowfoam or by ring closure of the 6-chloro-5-hydroxy fatty acids. The product yield of chloroalkoxy fatty acids is dependent on the nature and volume of the alcohol used in the reaction, as well as the concentration and pH of the sodium hypochlorite solution. Primary alcohols such as methanol and butanol produce maximal yields (50-60%) of chloroalkoxy fatty acids whereas the secondary alcohol 2-propanol gives a 30% yield. Chloroalkoxy fatty acid yields can be increased to 75-80% by elimination of water from the reaction mixture through a procedure that partitions sodium hypochlorite from water into hexane/ethyl acetate mixtures. All of the reaction products were fully characterized using nuclear magnetic resonance and gas chromatography-mass spectrometry. 

bleach; chloroalkoxy; chlorohydroxy; chlorolactone; 5,13-docosadienoic acid; 5-docosenoic acid; 13-docosenoic acid; 5-eicosenoic acid; meadowfoam fatty acids; sodium hypochlorite