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Dimethylformamide → HCID 67273752, Verbindung

HRID 1696735
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1696735
[S:1](=[O:4])(=O)=[O:2].C[N:6](C)C=O.[CH2:10]([C:14]1[S:15][CH:16]=[CH:17][C:18]=1[CH3:19])[CH:11]([CH3:13])[CH3:12].S(Cl)(Cl)=O>ClCCl>[CH2:10]([C:14]1[S:15][C:16]([S:1]([NH2:6])(=[O:4])=[O:2])=[CH:17][C:18]=1[CH3:19])[CH:11]([CH3:13])[CH3:12]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 24682Sulfur trioxideHCID 10241021HCID 10241021, Verbindung

Produkt 1

HCID 67273752HCID 67273752, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a mixture of 0.368 g of the complex of sulfur trioxide with dimethylformamide in 1.5 ml dichloromethane was added 0.309 g 2-isobutyl-3-methyl-thiophene and the mixture was heated to 55° C. for 30 min. and to 80° C. for an other 30 min. The mixture was cooled to room temperature and 0.286 g thionylchloride was added. The mixture was heated to 55° C. for ca 30 min cooled to room temperature and poored onto ice and extracted with ethyl acetate, the phases were separated and the organic phase was washed with water and brine and evaporated. The residue was taken up in 10 ml acetone and mixed with 1 ml 25% aqueous ammonia for ca 30 min. The reaction mixture was partitioned between water and ethyl acetate. The phases were separated and the organic phase was purified by chromatography on silica gel with ethyl acetate:heptane=1:3 to yield 0.16 g of the title compound as oil. MS (ISN) M−H+=232.0

Aufarbeitung

  1. temperatureThe mixture was cooled to room temperature
  2. temperatureThe mixture was heated to 55° C. for ca 30 min
  3. temperaturecooled to room temperature and poored onto ice
  4. extractionextracted with ethyl acetate
  5. customthe phases were separated
  6. washthe organic phase was washed with water and brine
  7. customevaporated
  8. additionmixed with 1 ml 25% aqueous ammonia for ca 30 min
  9. customThe reaction mixture was partitioned between water and ethyl acetate
  10. customThe phases were separated
  11. customthe organic phase was purified by chromatography on silica gel with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-86fe7fe0b98c49f6b21c34fa85a6dbcc
Quelldatensatz
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08163778B2

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