Reacción #674299
ord-5da05256bf684a199f4b4b90ac122670
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1OtroTo the mixture thus obtained
- 2workup.STIRRINGThe mixture was stirred at room temperature overnight
- 3workup.ADDITIONafter addition
- 4workup.STIRRINGTo the reaction mixture stirred in an external ice-bath
- 5workup.ADDITIONAfter addition
- 6workup.STIRRINGthe mixture was stirred at room temperature for 4 h
- 7Filtraciónfiltered
- 8Otroto remove the solid
- 9OtroThe phases were separated
- 10ExtracciónThe aqueous phase was extracted with EtOAc
- 11LavadoThe combined organic phase was washed with brine
- 12Secadodried over anhydrous Na2SO4
- 13Concentraciónconcentrated
- 14Otroto give the residue which
- 15Otrowas purified by CombiFlash (40 g silica gel column, EtOAc/Hexane: 0-40%)
Procedimiento
To a flame-dried RB flask with tert-butyl 4-methylenepiperidine-1-carboxylate (2.96 g, 15 mmol, 1.0 equiv) and Zn/Cu couple (6.54 g, 172.5 mmol, 11.5 equiv) under vacuum, t-BuOMe (60 mL) was charged and refilled the flask with N2 balloon. To the mixture thus obtained stirred at 15° C., a solution of 2,2,2-trichloroacetyl chloride in DME (20 mL) was added dropwise. The mixture was stirred at room temperature overnight after addition. To the reaction mixture stirred in an external ice-bath, a saturated solution of NH4Cl (60 mL) was added slowly and carefully (especially the first few drops). After addition, the mixture was stirred at room temperature for 4 h, filtered to remove the solid. The phases were separated. The aqueous phase was extracted with EtOAc. The combined organic phase was washed with brine, dried over anhydrous Na2SO4, concentrated to give the residue which was purified by CombiFlash (40 g silica gel column, EtOAc/Hexane: 0-40%) to afford 619 mg (15%) of tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate.