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Diethyl Ether → 3-Butylfuran

HRID 507344
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 507344
C([Li])(C)(C)C.[CH3:6][CH2:7][CH2:8][CH2:9]C.[CH3:11][CH2:12][O:13][CH2:14][CH3:15]>>[CH2:6]([C:11]1[CH:15]=[CH:14][O:13][CH:12]=1)[CH2:7][CH2:8][CH3:9]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 3283Diethyl EtherHCID 8003PentaneHCID 178418306HCID 178418306, Verbindung

Produkt 1

HCID 122242583-ButylfuranAusbeute 100 %

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

The iodo-product obtained from Step B above (2.2 g, 8.8 mmol) was dissolved in 60 mL of ether, and stirred in a −78° C. bath. A 1.7 M solution of t-butyllithium in pentane (10.4 mL, 17.7 mmol) was added dropwise. After 20 min, cooling bath was removed. Reaction was continued for 2.5 hr and quenched with H2O (20 mL). The aqueous mixture was stirred overnight and separated. The aqueous layer was extracted with ether (30 mL). The combined organic layers were washed with brine, dried by Na2SO4, and filtered through a Celite pad. Removal of solvent gave 1.10 g (100%) of 3-butylfuran as a reddish-yellow oil.

Aufarbeitung

  1. temperaturecooling bath
  2. customwas removed
  3. customReaction
  4. waitwas continued for 2.5 hr
  5. customquenched with H2O (20 mL)
  6. stirringThe aqueous mixture was stirred overnight
  7. customseparated
  8. extractionThe aqueous layer was extracted with ether (30 mL)
  9. washThe combined organic layers were washed with brine
  10. dry with materialdried by Na2SO4
  11. filtrationfiltered through a Celite pad
  12. customRemoval of solvent

Quellen und Nachweise

ORD-Eintrag
ord-4c448dcadcf34e2dbd61f571b30ef65b
Quelldatensatz
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07786149B2

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