Reacción #2254195
ord-4f46c7938f6a486eadb46693249fcfea
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otroa 50-mL, one-necked, round-bottom flask equipped with a magnetic stirrer
- 2workup.STIRRINGThe reaction mixture was stirred at room temperature under nitrogen for 5 minutes
- 3workup.STIRRINGstirred overnight
- 4OtroThe progress of reaction
- 5OtroAfter completion of the reaction
- 6Filtraciónthe reaction mixture was filtered through a bed of silica gel (˜15 g)
- 7OtroThe filtrate was evaporated in vacuo
- 8Otroto obtain a crude compound
- 9OtroThis was purified by column chromatography
- 10Lavadoto elute the product from the column
- 11workup.ADDITIONAll fractions containing the desired pure product
- 12Concentraciónconcentrated in vacuo
Procedimiento
a 50-mL, one-necked, round-bottom flask equipped with a magnetic stirrer and stir bar was charged with 9-methoxy-nonanol (1.0 g, 5.9 mmol), dichloromethane (10 mL), molecular sieves (1.0 g, 3 A), sodium acetate (0.1 g) at room temperature. The reaction mixture was stirred at room temperature under nitrogen for 5 minutes. The reaction mixture was charged with pyridinium dichromate (4.7 g, 12.5 mmol) and stirred overnight. The progress of reaction was monitored by TLC (Note 1). After completion of the reaction, the reaction mixture was filtered through a bed of silica gel (˜15 g). The filtrate was evaporated in vacuo to obtain a crude compound. This was purified by column chromatography using silica gel column (250-400 mesh, 40 g). A solvent gradient of ethyl acetate in hexane (10-50%) was used to elute the product from the column. All fractions containing the desired pure product were combined and concentrated in vacuo to give pure 9-methoxy-nonanal (lot D-1027-156, 553 mg, 54.4%). Completion of the reaction was monitored by thin layer chromatography (TLC) using a thin layer silica gel plate; eluent: 60% ethyl acetate in hexanes.