Reacción #1563925

Ecuación de reacción

EtOAc

K2CO3

β-bromophenetole

methyl (R)-piperidine-2-carboxylate

→

title compound

Rendimiento 64.0%

methyl (R)-1-(2-phenoxyethyl)piperidine-2-carboxylate

Rendimiento 64.0%

Disolventes

DMF

Condiciones de reacción

Tratamiento posterior

1. 1
   TemperaturaCool the mixture to room temperature
2. 2
   LavadoWash the organic phase with water (4×100 mL) and saturated aqueous NaCl (100 mL)
3. 3
   SecadoDry the organic phase over K2CO3
4. 4
   Filtraciónfilter
5. 5
   Otroto remove the solids
6. 6
   Concentraciónconcentrate the filtrate under reduced pressure
7. 7
   Otroto furnish a yellow oil
8. 8
   ConcentraciónConcentrate the fractions
9. 9
   workup.ADDITIONcontaining the desired product under reduced pressure

Procedimiento

Dissolve methyl (R)-piperidine-2-carboxylate (5.00 g, 34.9 mmol) in DMF (87 mL) and treat with K2CO3 (14.48 g, 104.8 mmol) and β-bromophenetole (7.16 g, 34.9 mmol). Stir the mixture overnight at 100° C. Cool the mixture to room temperature and add EtOAc (250 mL). Wash the organic phase with water (4×100 mL) and saturated aqueous NaCl (100 mL). Dry the organic phase over K2CO3, filter to remove the solids, and concentrate the filtrate under reduced pressure to furnish a yellow oil. Subject this crude material to flash chromatography on silica gel eluting with a gradient of 20% to 100% EtOAc/hexanes. Concentrate the fractions containing the desired product under reduced pressure to furnish the title compound as a colorless oil in ca. 90% purity by 1H NMR analysis (6.50 g, 64% yield). Mass spectrum (m/z) 264 (M+H)+. 1H NMR (400 MHz, CDCl3): δ 7.27 (dd, J=8.5, 7.3 Hz, 2H), 6.93 (t, J=7.3 Hz, 1H), 6.88 (d, J=8.8 Hz, 2H), 4.10 (app t, J=6.1 Hz, 2H), 3.72 (s, 3H), 3.29 (dd, J=8.4, 4.0 Hz, 1H), 3.14 (app dt, J=11.3, 6.4 Hz, 1H), 2.95 (app dt, J=13.7, 6.1 Hz, 1H), 2.89 (app dt, J=13.7, 6.1 Hz, 1H), 2.42 (ddd, J=11.6, 7.9, 3.7 Hz, 1H), 1.90-1.82 (m, 1H), 1.79 (app td, J=8.9, 3.8 Hz, 1H), 1.67-1.59 (m, 3H), 1.39 (app td, J=8.8, 4.0 Hz, 1H).

Fuente