Reacción #74293
ord-dc1e615057304224a797f221d68e1d21
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Lavadowashed with 3 mL 1N HCl
- 2SecadoThe organic phase was dried with MgSO4
- 3Filtraciónfiltered into a reaction vessel
- 4OtroThe solution was placed in an ice-water bath
- 5workup.ADDITIONN-hydrosuccinimide (82 mg) then dicyclohexylcarbodiimide (1.3 mL of a 0.5 M solution in dichloromethane) were added
- 6Temperaturawith warming for 8 hours
- 7workup.ADDITIONAt this time propyl amine (40 mg) was added as a neat liquid
- 8workup.STIRRINGto stir at room temperature overnight
- 9FiltraciónThe reaction was filtered
- 10Otroevaporated
Procedimiento
DMRIE-Ox (300 mg) was dissolved in 7 mL chloroform and washed with 3 mL 1N HCl. The organic phase was dried with MgSO4, then filtered into a reaction vessel. The solution was placed in an ice-water bath and N-hydrosuccinimide (82 mg) then dicyclohexylcarbodiimide (1.3 mL of a 0.5 M solution in dichloromethane) were added and the reaction was allowed to stir with warming for 8 hours. At this time propyl amine (40 mg) was added as a neat liquid and the reaction allowed to stir at room temperature overnight. The reaction was filtered, then evaporated. Chromatography of the filtrate residue through silica gel with CHCl3:MeOH:NH4OH:H2O (90:10:0.25:0.25) afforded pure product.