1-Bromo-3-methylbutane → Thiophene, 2-isopentyl-

HRID 235093

Reaktionsgleichung

Reaktionsgleichung von HRID 235093
[CH2:1](Br)[CH2:2][CH:3]([CH3:5])[CH3:4].[Li][C:8]1[S:9][CH:10]=[CH:11][CH:12]=1>O>[CH3:4][CH:3]([CH3:5])[CH2:2][CH2:1][C:8]1[S:9][CH:10]=[CH:11][CH:12]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Isopentyl bromide (Aldrich, 8 g, 53mmol) was added to 53 mL of an ice-cooled solution of lithiothiophene (1.0M in THF, 53 mmol). The reaction was stirred at 0° C. for 2 hours, at room temperature for 16 hours, and poured into water, then the mixture was extracted with hexane. The organic layer was dried and concentrated, and the residue was purified by column chromatography on silica gel, eluting with hexane, to give 7.2 g (88% yield) of the title compound as a colorless oil. NMR (CDCl3) δ:7.10 (dd, J=1, 6 Hz, 1H), 6.90 (dd, J=4, 6 Hz, 1H), 6.78 (dd, J=1, 4 Hz, 1H), 2.84 (t, J=8 Hz, 2H), 1.7-1.5 (m, 3H), 0.94 (d, J=6 Hz, 6H).

Aufarbeitung

  1. extractionthe mixture was extracted with hexane
  2. customThe organic layer was dried
  3. concentrationconcentrated
  4. customthe residue was purified by column chromatography on silica gel
  5. washeluting with hexane

Quellen und Nachweise

ORD-Eintrag
ord-524b9e03480a4f4b83c07433c4943f12
Quelldatensatz
uspto-grants-1997_01
Patentnummer
US05597832

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