تفاعل #502078
ord-a124b7fabb02462cb655ee245bf1f3b1
معادلة التفاعل
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىfitted with thermocouple, magnetic stirrer and condenser
- 2درجة الحرارةThe reaction mixture was refluxed for 2 hrs
- 3درجة الحرارةcooled
- 4أخرىThe crude reaction mixture
- 5استخلاصwas extracted with hexane (4×100 mL)
- 6تجفيفthe combined organic phase dried over magnesium sulphate
- 7ترشيحfiltered
- 8أخرىthe solvent removed in vacuo
- 9أخرىThe crude product was chromatographed over silica gel (hexane/methyltert-butyl ether)
الإجراء التجريبي
{4-[(1,5-dimethylhexyl)oxy]butyl}-1,3-dioxolane (1.4 g, 43% pure by GC RPA, 3.9 mmol), acetic acid (10 mL), tetrahydrofuran (16 mL) and water (20 mL) were added to a 100 mL three-necked flask fitted with thermocouple, magnetic stirrer and condenser. The reaction mixture was refluxed for 2 hrs, cooled and saturated sodium carbonate (150 mL) added. The crude reaction mixture was extracted with hexane (4×100 mL), the combined organic phase dried over magnesium sulphate, filtered and the solvent removed in vacuo. The crude product was chromatographed over silica gel (hexane/methyltert-butyl ether) to yield pure 5-[(1,5-dimethylhexyl)oxy]pentanal as a colourless oil (0.22 g, 1.02 mmol, chemical yield 26%).