반응 #502078

ord-a124b7fabb02462cb655ee245bf1f3b1

반응 방정식

O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CC(C)CCCC(C)OCCCCC1OCCO1
{4-[(1,5-dimethylhexyl)oxy]butyl}-1,3-dioxolane
CC(=O)O
acetic acid
C1CCOC1
tetrahydrofuran
CC(C)CCCC(C)OCCCCC=O
5-[(1,5-dimethylhexyl)oxy]pentanal
수율 26.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타fitted with thermocouple, magnetic stirrer and condenser
  2. 2
    온도The reaction mixture was refluxed for 2 hrs
  3. 3
    온도cooled
  4. 4
    기타The crude reaction mixture
  5. 5
    추출was extracted with hexane (4×100 mL)
  6. 6
    건조the combined organic phase dried over magnesium sulphate
  7. 7
    여과filtered
  8. 8
    기타the solvent removed in vacuo
  9. 9
    기타The crude product was chromatographed over silica gel (hexane/methyltert-butyl ether)

실험 절차

{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%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08088725B2uspto-grants-2012_01