Methyl levulinate → methyl 2-(5-methoxy-2-methyl-1H-indol-3-yl)acetate

HRID 1683985

Reaktionsgleichung

Reaktionsgleichung von HRID 1683985
Cl.[CH3:2][O:3][C:4]1[CH:9]=[CH:8][C:7]([NH:10]N)=[CH:6][CH:5]=1.O=[C:13]([CH3:20])[CH2:14][CH2:15][C:16]([O:18][CH3:19])=[O:17]>CC(O)=O>[CH3:2][O:3][C:4]1[CH:9]=[C:8]2[C:7](=[CH:6][CH:5]=1)[NH:10][C:13]([CH3:20])=[C:14]2[CH2:15][C:16]([O:18][CH3:19])=[O:17]

Komponenten

4

Edukt 2

HCID 69354Methyl levulinateHCID 27239044-Methoxyphenylhydrazine hydrochloride

Produkt 1

HCID 82067methyl 2-(5-methoxy-2-methyl-1H-indol-3-yl)acetate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

A suspension of 4-methoxyphenyl hydrazine hydrochloride (50 g, 0.286M) and methyl 4-oxo-pentanoate (40 mL, 0.315M) in HOAc (500 mL) was stirred for 16 h at reflux. The solvent was removed under vacuum, and the brown residue was partitioned between EtOAc and saturated NaHCO3 solution. The organic layer was washed with H2O and brine, and was then dried (MgSO4) and filtered. Following removal of the solvent, the crude product was purified by flash chromatography (1:20 EtOAc/toluene), to give 48 g of the title compound as a pale brown syrup.

Aufarbeitung

  1. temperatureat reflux
  2. customThe solvent was removed under vacuum
  3. customthe brown residue was partitioned between EtOAc and saturated NaHCO3 solution
  4. washThe organic layer was washed with H2O and brine
  5. dry with materialwas then dried (MgSO4)
  6. filtrationfiltered
  7. customremoval of the solvent
  8. customthe crude product was purified by flash chromatography (1:20 EtOAc/toluene)

Quellen und Nachweise

ORD-Eintrag
ord-9502270d9d9e4323969f7d6d0f4163d5
Quelldatensatz
uspto-grants-1997_06
Patentnummer
US05639780

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