Reacción #84048
ord-0186fe48a824439e807128658024c08c
Ecuación de reacción
quinuclidin-3-one hydrochloride
sodium methoxide
→
title compound
Quinuclidin-3-one
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1FiltraciónThe resulting precipitate is filtered off with suction
- 2Concentraciónthe filtrate is concentrated in vacuo
- 3OtroThe residue is partitioned between chloroform and water
- 4Extracciónextracted with chloroform
- 5SecadoThe combined organic phases are dried over sodium sulfate
- 6Concentraciónconcentrated in vacuo
Procedimiento
100 g (0.62 mol) of quinuclidin-3-one hydrochloride are suspended in 2 l of methanol. At 0° C., a solution of 33.4 g (0.62 mol) of sodium methoxide in 250 ml of methanol is slowly added dropwise. The mixture is stirred at room temperature for 16 h. The resulting precipitate is filtered off with suction, and the filtrate is concentrated in vacuo. The residue is partitioned between chloroform and water and extracted with chloroform. The combined organic phases are dried over sodium sulfate and concentrated in vacuo. 58.8 g (75.9% of theory) of the title compound are obtained.