Reacción #1833207
ord-7f334a8b5b6a49dd9460fa837145c1d5
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroThe reaction was quenched
- 2workup.ADDITIONby adding water
- 3Otrothe organic layer was separated
- 4Extracciónthe aqueous layer was extracted with dichloromethane (3×25 mL)
- 5LavadoThe combined organic layer was washed with brine
- 6Secadodried over Na2SO4
- 7Concentraciónconcentrated in vacuo to orange colored slush
- 8workup.ADDITIONTo this was added about 15 mL of dichloromethane and refrigerated overnight
Procedimiento
4-methoxy-2,3-dinitrobenzaldehyde (2.94 mmol) and 3,4,5-trimethoxybenzyltriphenyl phosphonium bromide (1.54 g, 2.94 mmol, 1.0 equiv) in anhydrous dichloromethane (25 mL) was added NaH (0.424 g, 17.67 mmol, 6.0 equiv). The reaction mixture was stirred at room temperature for about 7 hours and monitored by TLC. The reaction was quenched by adding water, the organic layer was separated and the aqueous layer was extracted with dichloromethane (3×25 mL). The combined organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo to orange colored slush. To this was added about 15 mL of dichloromethane and refrigerated overnight. The crude mixture was subjected to flash chromatography to isolate 2′,3′-Dinitro-3,4,4′,5-tetramethoxy-(Z)-stilbene (0.581 g, 1.48 mmol, 51%, solid)