Butyl bromide → n-Butyl cyclopentadiene

HRID 476287Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 476287
Br[CH2:2][CH2:3][CH2:4][CH3:5].[CH:6]1([Mg]Cl)[CH:10]=[CH:9][CH:8]=[CH:7]1>>[CH2:2]([C:10]1[CH2:9][CH:8]=[CH:7][CH:6]=1)[CH2:3][CH2:4][CH3:5]

Komponenten

3

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To 1-bromobutane (105 g, 0.766 mol) was added cyclopentadienyl magnesium chloride (800 mL of 1M solution in THF, 0.8 mol) at 0° C. in 20 minutes. After stirring for an additional 2 hours at 0° C., the mixture was warmed to room temperature. After stirring overnight, the reaction was quenched with a mixture of ice and water. The mixture was extracted with pentane. The organic layer was washed with water and dried over anhydrous sodium sulfate. Removal of the solvent under vacuum at room temperature gave a brown liquid (85 g, crude butylcyclopentadiene). To the crude butylcyclopentadiene (75 g) dissolved in methanol (500 mL) was added acetone (54 mL) followed by pyrrolidine (63 mL) at 0° C. The mixture was warmed up to room temperature and stirred for 24 hours. The reaction was quenched with a mixture of ice and acetic acid. The mixture was extracted with pentane. The organic layer was washed with water and dried over anhydrous sodium sulfate. Removal of the solvent under vacuum gave the desired product (89 g) as a brown liquid.

Aufarbeitung

  1. temperaturethe mixture was warmed to room temperature
  2. stirringAfter stirring overnight
  3. customthe reaction was quenched with a mixture of ice and water
  4. extractionThe mixture was extracted with pentane
  5. washThe organic layer was washed with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. customRemoval of the solvent under vacuum at room temperature

Quellen und Nachweise

ORD-Eintrag
ord-15221f30884e4f7f808cb137022124c5
Quelldatensatz
uspto-grants-2014_01
Patentnummer
US08637691B2

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