C(Br)(C)(C)C.[C:6]([OH:11])(=[O:10])[CH:7]([CH3:9])[OH:8].C(=O)(O)[O-].[Na+].O.[CH3:18][S:19]([CH3:21])=O>>[CH3:18][S:19][CH2:21][O:10][C:6](=[O:11])[CH:7]([CH3:9])[OH:8]153 ml (1.1 mol) of tert.butyl bromide are slowly added dropwise to a suspension of 10 g (0.11 mol) of L (+)-lactic acid and 94.2 g (1.1 mol) of sodium bicarbonate in 200 ml of dimethyl sulphoxide. The mixture is stirred for 48 hours, then poured into 1 liter of water and extracted twice with 100 ml of ethyl acetate each time. The organic phase is back-washed three times with 200 ml of water each time and subsequently evaporated. The crude product is chromatographed on a 20-fold amount of silica gel with n-hexane/ethyl acetate (4:1) and the eluate is evaporated. There are obtained 5.7 g of L (-)-lactic acid [(methylthio)methyl] ester; [α]D20 =-39.27° (c=1.3% in chloroform).
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