(2S)-2-amino-2-(4-fluorophenyl)ethanol

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

Procedure: Proceeding as described for (45), but using (S)-2-amino-2-(4-fluorophenyl)ethanol and 3-trifluoromethylbenzenesulfonyl chloride afforded (S)-2-(4-fluorophenyl)-2-(3-(trifluoro-methyl)benzenesulfonamido)ethyl 3-(trifluoromethyl)benzenesulfonate (47). MS m/z: 572.3 (M+H) (Calc'd for C22H16F7NO5S2: 571.48).

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

Procedure: Proceeding as described for (45), but using (S)-2-amino-2-(4-fluorophenyl)ethanol and 3-trifluoromethylbenzenesulfonyl chloride afforded (S)-2-(4-fluorophenyl)-2-(3-(trifluoro-methyl)benzenesulfonamido)ethyl 3-(trifluoromethyl)benzenesulfonate (47). MS m/z: 572.3 (M+H) (Calc'd for C22H16F7NO5S2: 571.48).

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

Procedure: Proceeding as described for (45), but using (S)-2-amino-2-(4-fluorophenyl)ethanol and 3-trifluoromethylbenzenesulfonyl chloride afforded (S)-2-(4-fluorophenyl)-2-(3-(trifluoro-methyl)benzenesulfonamido)ethyl 3-(trifluoromethyl)benzenesulfonate (47). MS m/z: 572.3 (M+H) (Calc'd for C22H16F7NO5S2: 571.48).

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

Procedure: To a 150 mL flame dry round bottom flask was added LiAlH4 (1.14 g, 29.9 mmol) and 70 mL THF. The solution was cooled to 0° C. and (S)-2-amino-2-(4-fluorophenyl)acetic acid (2.53 g, 15.0 mmol) was added portionwise. Following the addition, the reaction mixture was heated to reflux under N2 for 20 h. The resulting mixture was then cooled to 0° C. and quenched slowly with 5% NaHCO3. The solvents were removed and the residue was suspended in EtOAc. After 2 h, the white precipitate was filtered and the filtrate concentrated to give the title compound. MS (m/z): 156.3 (M+H) (Calc'd for C8H10FNO: 155.17). To a 150 mL flame dry round bottom flask the addition the reaction mixture was heated to reflux under N2 for 20 h The resulting mixture was then cooled to 0° C. quenched slowly with 5% NaHCO3 The solvents were removed the white precipitate was filtered the filtrate concentrated

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

Procedure: To a 150 mL flame dry round bottom flask was added LiAlH4 (1.14 g, 29.9 mmol) and 70 mL THF. The solution was cooled to 0° C. and (S)-2-amino-2-(4-fluorophenyl)acetic acid (2.53 g, 15.0 mmol) was added portionwise. Following the addition, the reaction mixture was heated to reflux under N2 for 20 h. The resulting mixture was then cooled to 0° C. and quenched slowly with 5% NaHCO3. The solvents were removed and the residue was suspended in EtOAc. After 2 h, the white precipitate was filtered and the filtrate concentrated to give the title compound. MS (m/z): 156.3 (M+H) (Calc'd for C8H10FNO: 155.17). To a 150 mL flame dry round bottom flask the addition the reaction mixture was heated to reflux under N2 for 20 h The resulting mixture was then cooled to 0° C. quenched slowly with 5% NaHCO3 The solvents were removed the white precipitate was filtered the filtrate concentrated