(2S)-2-amino-2-(2-chlorophenyl)ethanol;hydrochloride

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of (S)-2-amino-2-(2-chlorophenyl)ethanol hydrochloride (500 mg, 2.40 mmol) in water (12 mL) at 0° C. was added potassium hydroxide (809 mg, 14.4 mmol) followed by THF (12 mL) and the reaction was stirred at 0° C. for 20 minutes. Bis(trichloromethyl) carbonate (713 mg, 2.40 mmol) was added and the reaction was stirred at 0° C. for 2 hours. The reaction was poured into EtOAc and the organic phase washed with 1N HCl, 1N NaOH and brine. The organic layer was dried over MgSO4, filtered and concentrated to provide (S)-4-(2-chlorophenyl)oxazolidin-2-one (265 mg, 55.8% yield) as an oil which solidified upon standing. the reaction was stirred at 0° C. for 2 hours the organic phase washed with 1N HCl, 1N NaOH and brine The organic layer was dried over MgSO4 filtered concentrated

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of (S)-2-amino-2-(2-chlorophenyl)ethanol hydrochloride (500 mg, 2.40 mmol) in water (12 mL) at 0° C. was added potassium hydroxide (809 mg, 14.4 mmol) followed by THF (12 mL) and the reaction was stirred at 0° C. for 20 minutes. Bis(trichloromethyl) carbonate (713 mg, 2.40 mmol) was added and the reaction was stirred at 0° C. for 2 hours. The reaction was poured into EtOAc and the organic phase washed with 1N HCl, 1N NaOH and brine. The organic layer was dried over MgSO4, filtered and concentrated to provide (S)-4-(2-chlorophenyl)oxazolidin-2-one (265 mg, 55.8% yield) as an oil which solidified upon standing. the reaction was stirred at 0° C. for 2 hours the organic phase washed with 1N HCl, 1N NaOH and brine The organic layer was dried over MgSO4 filtered concentrated

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of (S)-2-amino-2-(2-chlorophenyl)ethanol hydrochloride (500 mg, 2.40 mmol) in water (12 mL) at 0° C. was added potassium hydroxide (809 mg, 14.4 mmol) followed by THF (12 mL) and the reaction was stirred at 0° C. for 20 minutes. Bis(trichloromethyl) carbonate (713 mg, 2.40 mmol) was added and the reaction was stirred at 0° C. for 2 hours. The reaction was poured into EtOAc and the organic phase washed with 1N HCl, 1N NaOH and brine. The organic layer was dried over MgSO4, filtered and concentrated to provide (S)-4-(2-chlorophenyl)oxazolidin-2-one (265 mg, 55.8% yield) as an oil which solidified upon standing. the reaction was stirred at 0° C. for 2 hours the organic phase washed with 1N HCl, 1N NaOH and brine The organic layer was dried over MgSO4 filtered concentrated