Facile synthesis of (R)-4-mercaptopyrrolidine-2-thione from L-aspartic acid

An SN2-type of substitution of (S)-bromide 4, which had been prepared from L-aspartic acid, with potassium thiobenzoate provided (R)-benzoylthio deriv ative 5 with complete inversion of the configuration. Compound 5 was conver ted, via iodide 6c, to (R)-4-amino-3-benzoylthiobutyric acid 8b. (R)-4-Merc aptopyrrolidine-2-thione 1 was readily obtained from 8b through cyclization with acetic anhydride, thionation with Lawesson's reagent and facile remov al of the S-benzoyl group with sodium methoxide.