Реакция #46639

Уравнение реакции

(S)-1-phenylethyl(R)-2-(4-hydroxy-4-methylpiperidin-1-yl)-2-phenylacetate

trifluoroacetic acid

→

title compound

Выход 98.7%

(R)-2-(4-Hydroxy-4-methylpiperidin-1-yl)-2-phenylacetic acid

Выход 98.7%

Растворители

dichloromethane

Условия реакции

Обработка

1. 1
   ДругоеThe volatiles were subsequently removed in vacuo
2. 2
   Другоеthe residue was purified by reverse-phase preparative HPLC (Primesphere C-18, 20×100 mm

Методика

To a solution of (S)-1-phenylethyl(R)-2-(4-hydroxy-4-methylpiperidin-1-yl)-2-phenylacetate (0.185 g, 0.52 mmol) in dichloromethane (3 mL) was added trifluoroacetic acid (1 mL) and the mixture was stirred at room temperature for 2 hours. The volatiles were subsequently removed in vacuo and the residue was purified by reverse-phase preparative HPLC (Primesphere C-18, 20×100 mm; CH3CN—H2O-0.1% TFA) to give the title compound (as TFA salt) as a pale bluish solid (0.128 g, 98%). LCMS: Anal. Calcd. for C14H19NO3: 249. found: 250 (M+H)+.

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