Methanol → methyl 1-methyl-1H-indole-7-carboxylate

HRID 1067767Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1067767
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[C:11]([OH:13])=[O:12])[CH:4]=[CH:3]1.S(Cl)(Cl)=O.[CH3:18]O>>[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[C:11]([O:13][CH3:18])=[O:12])[CH:4]=[CH:3]1

Komponenten

4

Versuchsvorschrift

To 70 ml of a methanol solution of 1.82 g (10.4 mmol) of 1-methyl-7-indolecarboxylic acid was added dropwise 3.09 g (26.0 mmol) of thionyl chloride at 0° C. The reaction mixture was refluxed for 2 hours and the solvent was then distilled off under reduced pressure. Ice water was poured onto the resulting residue and ammonium hydroxide was added to render the mixture alkaline. The mixture was extracted three times with ethyl acetate. The combined extracts were washed with water and dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure. The residue was isolated and purified by silica gel column chromatography to give 1.16 g (59.0%) of methyl 1-methyl-7-indolecarboxylate.

Aufarbeitung

  1. temperatureThe reaction mixture was refluxed for 2 hours
  2. distillationthe solvent was then distilled off under reduced pressure
  3. additionIce water was poured onto the resulting residue and ammonium hydroxide
  4. additionwas added to render the mixture alkaline
  5. extractionThe mixture was extracted three times with ethyl acetate
  6. washThe combined extracts were washed with water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. distillationThe solvent was then distilled off under reduced pressure
  9. customThe residue was isolated
  10. custompurified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-4e5ff870f7ce45139de9dd7237a199c7
Quelldatensatz
uspto-grants-2001_06
Patentnummer
US06248772B1

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