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Diethyl Ether → 4-Bromo-3,5-dimethylthiophene-2-carbaldehyde

HRID 904476
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 904476
Br[C:2]1[S:3][C:4]([CH3:9])=[C:5]([Br:8])[C:6]=1[CH3:7].C[CH2:11][O:12]CC.C([Li])CCC>CN(C)C=O>[Br:8][C:5]1[C:6]([CH3:7])=[C:2]([CH:11]=[O:12])[S:3][C:4]=1[CH3:9]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 3283Diethyl EtherHCID 105880762,4-Dibromo-3,5-dimethylthiopheneHCID 178418339Butyllithium

Produkt 1

HCID 128752694-Bromo-3,5-dimethylthiophene-2-carbaldehyde

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
-35 °C

Versuchsvorschrift

15.0 G. of 2,4-dibromo-3,5-dimethylthiophene was dissolved in 250 ml. of anhydrous ether and cooled to -70° C. with stirring under argon. 24 Ml. of a 2.4 M solution of n-butyl lithium was slowly added to the solution and the mixture was warmed to -35° C. for 10 minutes, and then cooled again to -70° C. 7.3 G. of dimethylformamide was added slowly to the mixture and the reaction mixture was warmed to room temperature for 14 hours. The resulting solution was poured into ice water, stirred for 20 minutes and extracted with ethyl ether. The ether extracts were combined, washed with an aqueous solution of 5% sodium carbonate, saturated sodium chloride solution, dried with sodium sulfate, filtered and evaporated to yield 4-bromo-3,5-dimethylthiophene-2-carboxaldehyde, m.p. 44°-45° C.

Aufarbeitung

  1. temperaturecooled again to -70° C
  2. temperaturethe reaction mixture was warmed to room temperature for 14 hours
  3. stirringstirred for 20 minutes
  4. extractionextracted with ethyl ether
  5. washwashed with an aqueous solution of 5% sodium carbonate, saturated sodium chloride solution
  6. dry with materialdried with sodium sulfate
  7. filtrationfiltered
  8. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-55bffb4672a94c2d9f2a5483a54753cc
Quelldatensatz
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04230872

Notizen zur Reaktion

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