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Diethyl Ether → HCID 67469124, Verbindung

HRID 1406303
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1406303
[Br:1][C:2]1[S:3][C:4]([CH:8]=[O:9])=[C:5]([CH3:7])[N:6]=1.C[Mg+].[Br-].[CH3:13]COCC>C1COCC1>[Br:1][C:2]1[S:3][C:4]([CH:8]([OH:9])[CH3:13])=[C:5]([CH3:7])[N:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 3283Diethyl EtherHCID 771748872-Bromo-4-methylthiazole-5-carbaldehydeHCID 178418689HCID 178418689, Verbindung

Produkt 1

HCID 67469124HCID 67469124, VerbindungAusbeute 87 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a mixture of 2-bromo-4-methylthiazole-5-carbaldehyde of preparation 98 (1.8 g, 8.8 mmol) in dry THF (50 mL) was added dropwise MeMgBr in Et2O (3M, 2.9 mL, 8.8 mmol) at −40° C. under N2. After the addition, the mixture was stirred at room temperature for 1 hr. TLC (petroleum ether/EtOAc=5:1) showed most of the starting material was consumed. To the reaction mixture was added saturated NH4Cl (60 mL). The mixture was extracted with EtOAc (50 mL×2). The combined organic layers were washed with brine (80 mL), dried over sodium sulfate and concentrated in vacuum. The residue was purified by a Biotage silica gel cartridge (EA/PE 48%, Rf=0.5) to give the title compound as a yellow oil (1.7 g, 87%).

Aufarbeitung

  1. additionAfter the addition
  2. customwas consumed
  3. additionTo the reaction mixture was added saturated NH4Cl (60 mL)
  4. extractionThe mixture was extracted with EtOAc (50 mL×2)
  5. washThe combined organic layers were washed with brine (80 mL)
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated in vacuum
  8. customThe residue was purified by a Biotage silica gel cartridge (EA/PE 48%, Rf=0.5)

Quellen und Nachweise

ORD-Eintrag
ord-204855a9873b4462a07b8ee0fc715e4b
Quelldatensatz
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08916593B2

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