3-Methyl-2-buten-1-OL → 2-[[(3-Methyl-2-butenyl)oxy]methyl]-5-nitrofuran

HRID 1779751Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1779751
[CH3:1][C:2]([CH3:6])=[CH:3][CH2:4][OH:5].[CH:7]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[O:9][C:8]=1[CH2:15]Br.C[C]C>[Ag]=O>[CH3:1][C:2]([CH3:6])=[CH:3][CH2:4][O:5][CH2:15][C:8]1[O:9][C:10]([N+:12]([O-:14])=[O:13])=[CH:11][CH:7]=1

Komponenten

5

Versuchsvorschrift

Freshly prepared silver oxide (34.8 g, 0.15 mol) was added to a mixture of 3-methyl-2-buten-1-ol (21.0 g, 25 mL, 0.24 mol) and 5-nitro-2-furfuryl bromide (18.8 g, 0.1 mol) and stirred at room temperature for 12 h. Silver salts were removed by filtration and the filter cake was washed with ether (200 mL). The filtrate and the washings were combined and evaporated to remove ether and excess 3-methyl-2-buten-1-ol. The oil obtained was purified by column chromatography (silica gel, hexane:ethyl acetate, 7:1). Fractions containing the product were collected and evaporated to give a light yellow oil. Yield 5.5 g. 1H NMR (CDCl3) ε 1.69 and 1.77 (s, 6H, CH3), 4.09 [d, 2H, (CH3)2C=CHCH2 --OCH2)], 4.64 [s, 2H, (CH3)2C=CHCH2 --OCH2)], 5.38 (t, 1H, (CH3)2C=CH--), 6.6 and 7.27 (d, 2H, ArH).

Aufarbeitung

  1. customSilver salts were removed by filtration
  2. washthe filter cake was washed with ether (200 mL)
  3. customevaporated
  4. customto remove ether and excess 3-methyl-2-buten-1-ol
  5. customThe oil obtained
  6. customwas purified by column chromatography (silica gel, hexane:ethyl acetate, 7:1)
  7. additionFractions containing the product
  8. customwere collected
  9. customevaporated
  10. customto give a light yellow oil

Quellen und Nachweise

ORD-Eintrag
ord-eff9cff50e924e058362933de8a3752b
Quelldatensatz
uspto-grants-1997_05
Patentnummer
US05627286

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