反应详情

4-(2-Carboxyphenyl)piperidine-1-carboxylic acid t-butyl ester (5.0 g, 160 mmol, 1.0 eq.) and THF (100 mL, 1.0 mol) were combined at room temperature under nitrogen. 1.0M Borane-THF complex in THF (32.7 mL, 32.7 mmol, 2.0 eq.) was added dropwise over 10 minutes (5° C. exotherm, gas evolution). The mixture was stirred at room temperature for 5 minutes, then heated at 50° C. for 1 hour. The mixture was cooled to room temperature, and the reaction was quenched slowly with MeOH (30 mL) (mild exotherm, significant gas evolution), then concentrated by rotary evaporation. The material was azeotroped with MeOH (2×50 mL). The crude product was dissolved in EtOAc (100 mL, 1 mol), washed with NaHCO3 (50 mL), then saturated aqueous NaCl (50 mL). The organic layer was dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to yield 4-(2-hydroxymethylphenyl)piperidine-1-carboxylic acid t-butyl ester (4.4 g) as a clear, light yellow oil that solidified upon sitting.

1. customwere combined at room temperature under nitrogen
2. temperatureheated at 50° C. for 1 hour
3. temperatureThe mixture was cooled to room temperature
4. customthe reaction was quenched slowly with MeOH (30 mL) (mild exotherm, significant gas evolution)
5. concentrationconcentrated by rotary evaporation
6. customThe material was azeotroped with MeOH (2×50 mL)
7. washwashed with NaHCO3 (50 mL)
8. dry with materialThe organic layer was dried over anhydrous Na2SO4
9. filtrationfiltered
10. concentrationconcentrated in vacuo