Réaction #420161

Équation de réaction

tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate

NaH

2,6-dinitrobenzonitrile

→

tert-butyl 2-((2-cyano-3-nitrophenoxy)methyl)piperidine-1-carboxylate

Rendement 70.6%

Solvants

water

THF

THF

DMF

Conditions de réaction

Traitement

1. 1
   Autre20 min
2. 2
   Autreat room temperature
3. 3
   Extractionextracted with EtOAc
4. 4
   Lavagethe combined organic phases were washed with brine
5. 5
   Séchagedried over MgSO4
6. 6
   Filtrationfiltered
7. 7
   Autreevaporated
8. 8
   AutreThe residue was purified by Biotage purification system (120 g Silicycle column, Hexane:EtOAc=3:2 as eluent)

Mode opératoire

To a solution of tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate (0.86 g, 4 mmol) in dry THF (30 mL) was added at −20° C. NaH (0.32 g, 8 mmol) and the mixture was stirred 10 min at −20° C. and then 20 min at room temperature. The reaction mixture was then cooled to −20° C. and 2,6-dinitrobenzonitrile (0.772 g, 4 mmol) in dry THF (10 mL) and DMF (1 mL) was added dropwise over 15 min period. The solution was stirred under nitrogen at room temperature for 18 hours, diluted with water and extracted with EtOAc, the combined organic phases were washed with brine, dried over MgSO4, filtered and evaporated. The residue was purified by Biotage purification system (120 g Silicycle column, Hexane:EtOAc=3:2 as eluent) to give tert-butyl 2-((2-cyano-3-nitrophenoxy)methyl)piperidine-1-carboxylate (1.02 g, 70.6%). MS 262 [M+H-Boc]+.

Source