تفاعل #2254195
ord-4f46c7938f6a486eadb46693249fcfea
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىa 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
- 4أخرىThe progress of reaction
- 5أخرىAfter completion of the reaction
- 6ترشيحthe reaction mixture was filtered through a bed of silica gel (˜15 g)
- 7أخرىThe filtrate was evaporated in vacuo
- 8أخرىto obtain a crude compound
- 9أخرىThis was purified by column chromatography
- 10غسيلto elute the product from the column
- 11workup.ADDITIONAll fractions containing the desired pure product
- 12تركيزconcentrated in vacuo
الإجراء التجريبي
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.