1-Bromododecane → 3-Dodecylthiophene

HRID 888670

Reaktionsgleichung

Reaktionsgleichung von HRID 888670
[Mg].Br[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].Br[C:16]1[CH:20]=[CH:19][S:18][CH:17]=1>CCOCC.Cl[Ni]1(Cl)[P](C2C=CC=CC=2)(C2C=CC=CC=2)CCC[P]1(C1C=CC=CC=1)C1C=CC=CC=1>[CH2:3]([C:16]1[CH:20]=[CH:19][S:18][CH:17]=1)[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]

Komponenten

6

Versuchsvorschrift

Dried ethyl ether (40 ml) was added to activated magnesium (1.22 g; 50 mmol), and 1-bromododecane (12.46 g; 50 mmol) was added thereto to prepare a Grignard reagent. Then, Ni(dppp)Cl2 (33 mg) was added thereto, and 3-bromothiophene (8 g; 49 mmol) dissolved in 10 ml of ether was slowly added dropwise. The reaction solution was refluxed for one day, and then a mixture of 2N HCl/ice (50 ml) was added to terminate the reaction. The resultant was extracted by using ethyl ether, and the solvent was distilled off under reduced pressure. The residue was dissolved in DMF (50 ml) and filtered to remove remaining paraffin. The filtrate was concentrated, and then the residue was distilled off under vacuum to obtain a colorless liquid of 3-dodecylthiophene (10.5 g; 85%).

Aufarbeitung

  1. additionwas added
  2. additionwas slowly added dropwise
  3. temperatureThe reaction solution was refluxed for one day
  4. additionwas added
  5. customto terminate
  6. customthe reaction
  7. extractionThe resultant was extracted
  8. distillationthe solvent was distilled off under reduced pressure
  9. dissolutionThe residue was dissolved in DMF (50 ml)
  10. filtrationfiltered
  11. customto remove
  12. concentrationThe filtrate was concentrated
  13. distillationthe residue was distilled off under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-07e923233ab444039188ad2166428110
Quelldatensatz
uspto-grants-2012_08
Patentnummer
US08247803B2

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