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Potassium Carbonate → 7-Ethynyl-2-methyl-quinoline

HRID 882081
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 882081
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][C:6]([C:12]#[C:13][Si](C)(C)C)=[CH:7][CH:8]=2)[N:3]=1.C([O-])([O-])=O.[K+].[K+]>CO>[C:12]([C:6]1[CH:5]=[C:4]2[C:9]([CH:10]=[CH:11][C:2]([CH3:1])=[N:3]2)=[CH:8][CH:7]=1)#[CH:13]
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Komponenten

4

Edukt 2

HCID 11430Potassium CarbonateHCID 673236902-Methyl-7-((trimethylsilyl)ethynyl)quinoline

Produkt 1

HCID 866838217-Ethynyl-2-methyl-quinolineAusbeute 86 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of 2-methyl-7-trimethylsilanylethynyl-quinoline (140 mg, 0.59 mmol, 1.0 eq) in solution in MeOH (5 mL) was added K2CO3 (324 mg, 2.34 mmol, 4 eq), and the resulting mixture was stirred overnight at room temperature. The solvent was then removed under reduced pressure and water was then added. The aqueous layer was extracted twice with cyclohexane, and then the combined organic layers were washed with brine and dried over MgSO4. After filtration and concentration under reduced pressure the crude product was purified by column chromatography on silica gel (Cyclohexane-EtOAc 99:1) to afford 84 mg of 7-ethynyl-2-methyl-quinoline as a yellow crystal (86%).

Aufarbeitung

  1. customThe solvent was then removed under reduced pressure and water
  2. additionwas then added
  3. extractionThe aqueous layer was extracted twice with cyclohexane
  4. washthe combined organic layers were washed with brine
  5. dry with materialdried over MgSO4
  6. filtrationAfter filtration and concentration under reduced pressure the crude product
  7. customwas purified by column chromatography on silica gel (Cyclohexane-EtOAc 99:1)

Quellen und Nachweise

ORD-Eintrag
ord-d9a98d205fe0459ba722a34f2e4179c2
Quelldatensatz
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08993767B2

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