تفاعل #502078

ord-a124b7fabb02462cb655ee245bf1f3b1

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىfitted with thermocouple, magnetic stirrer and condenser
  2. 2
    درجة الحرارةThe reaction mixture was refluxed for 2 hrs
  3. 3
    درجة الحرارةcooled
  4. 4
    أخرىThe crude reaction mixture
  5. 5
    استخلاصwas extracted with hexane (4×100 mL)
  6. 6
    تجفيفthe combined organic phase dried over magnesium sulphate
  7. 7
    ترشيحfiltered
  8. 8
    أخرىthe solvent removed in vacuo
  9. 9
    أخرىThe 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%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08088725B2uspto-grants-2012_01