Hydrochloric Acid → (3R)-3-{[tert-Butyl(dimethyl)silyl]oxy}-1-chlorobutan-2-one

Participants

Reaction Steps

A mixture of 5.00 g (21.52 mmol) of ethyl (R)-2-(tert-butyldimethylsilyloxy)propionate, 3.76 g (32.3 mmol) of sodium chloroacetate, 2.18 g (21.5 mmol) of triethylamine, and 50 mL of THF was cooled in ice, and 37 mL (64.6 mmol) of a 1.75 M solution of tert-butylmagnesium chloride was added dropwise thereto over a period of 1 hour. After the completion of the dropwise addition, the reaction was allowed to proceed at 0° C. for 3 hours, and 6 M hydrochloric acid (about 20 mL) was added to the reaction solution to adjust the pH to 6.0. Subsequently, stirring was performed at 25° C. for 2 hours. A product was extracted with ethyl acetate (100 mL×2). The resulting organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain 5.19 g of the title compound as a colorless oil (yield: 100%). 1H-NMR (400 MHz, CDCl3) δ: 0.10 (S, 6H), 0.92 (s, 9H), 1.24 (d, 3H, J=6.8 Hz), 4.35 (q, 1H, J=6.8 Hz), 5.50 (q, 2H, J=17.0 Hz).

Provenance & Evidence