Abstract
A series of (R)-(+)-ethyl aryloxypropionates (4a–4p) have been synthesized by the reaction of substituted phenols with ethyl (S)-(−)-tosyloxy lactate under the conditions of microwave irradiation and without solvents. The reaction conditions have been optimized. A good method for the preparation of (R)-(+)-ethyl aryloxypropionate was developed, with good yields, high enantiomer excess, short reaction times, easy workup, and simple procedure.
ACKNOWLEDGMENT
This work was financially supported by the Polish State Committee for Scientific Research Grant No. N N209 119937 and Warsaw Technical University.