Abstract
AbstractEnzyme‐catalyzed reactions in organic media of rac‐ketoprofen esters with different nucleophiles such as alcohols, amines, and water have been studied. Among the parameters optimized are the enzyme, the activated substrate, and the solvent. With the enzymes used in this study the preferred substrate was the trifluoroethyl ester of rac‐ketoprofen (rac‐2), whose (R)‐enantiomer reacted preferentially. The enzyme of choice was the lipase M‐AP‐10 from Mucor miehei and best results were obtained with diisopropyl ether as solvent. Three different methods have been scaled‐up for the resolution of 75–150 g of substrate: transesterification with 1‐butanol (90% yield of (S)‐ketoprofen, 88% ee), transesterification with 2‐(2‐pyridyl)ethanol (94% yield, 92% ee), and hydrolysis in wet organic solvent (93% yield, 97% ee). Despite the comparable chemical and optical yields obtained with these three methods, the use of 2‐(2‐pyridyl)ethanol and the hydrolysis allowed a much easier work‐up and isolation of the desired (+)‐(S)‐ketoprofen. © 1993 Wiley‐Liss, Inc.
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