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Ammonium Chloride → 2-Methyl-4-phenylthiophene

HRID 1868536
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1868536
[C:1]1([Mg]Br)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Br[C:10]1[CH:11]=[C:12]([CH3:15])[S:13][CH:14]=1.[NH4+].[Cl-]>CCOCC>[CH3:15][C:12]1[S:13][CH:14]=[C:10]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 25517Ammonium ChlorideHCID 6385844-Bromo-2-methylthiopheneHCID 178418255HCID 178418255, Verbindung

Produkt 1

HCID 114010612-Methyl-4-phenylthiophene

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

A solution of PhMgBr (prepared from 1.65 g of Mg (0.0678 mol) and 10.64 g of PhBr (0.0678 mol) in 40 mL of diethyl ether) was added to a mixture of 10 g (0.0565 mol) of 4-bromo-2-methylthiophene and 0.62 g (0.0012 mol) of NiCl2dppp in 50 mL of ether under stirring at reflux. The reaction mixture was refluxed for additional 3 h and then stirred overnight. The resulting mixture was treated with 10% aqueous NH4Cl, the organic layer was separated, washed with 10% aqueous NH4Cl and then dried with anhydrous Na2SO4. Solvent was evaporated, the residue was recrystallized from methanol. Yield 6.8 g (70%) of colorless crystals.

Aufarbeitung

  1. temperatureat reflux
  2. temperatureThe reaction mixture was refluxed for additional 3 h
  3. stirringstirred overnight
  4. customthe organic layer was separated
  5. washwashed with 10% aqueous NH4Cl
  6. dry with materialdried with anhydrous Na2SO4
  7. customSolvent was evaporated
  8. customthe residue was recrystallized from methanol

Quellen und Nachweise

ORD-Eintrag
ord-825e3846dd404120bf8c081d97851455
Quelldatensatz
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07635781B2

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