Reaktion #3202

ord-3dda300c17224ab9a94f5d53c331760a

Reaktionsgleichung

COC(=O)c1c(C)cccc1N
methyl 2-amino-6-methylbenzoate
COC(=O)C#CC(=O)OC
dimethyl acetylenedicarboxylate
CC(C)(C)[O-].[K+]
potassium t-butoxide
COC(=O)c1nc2cccc(C)c2c(O)c1C(=O)OC
title compound
Ausbeute 66.4%
COC(=O)c1nc2cccc(C)c2c(O)c1C(=O)OC
Dimethyl 4-hydroxy-5-methylquinoline-2,3-dicarboxylate
Ausbeute 66.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas refluxed fpr 18 hr under a nitrogen atmosphere
  2. 2
    Sonstigeformed
  3. 3
    TemperaturAfter refluxing this mixture for 1.5 hr
  4. 4
    Temperaturit was cooled to room temperature
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigeto separate the solids
  7. 7
    workup.DISSOLUTIONThe solids were dissolved in water
  8. 8
    Sonstigeto form a precipitate
  9. 9
    FiltrationThe mixture was filtered
  10. 10
    Waschenthe collected solids were washed with water
  11. 11
    Sonstigedried

Vorschrift

A stirred mixture of methyl 2-amino-6-methylbenzoate (1.50 g, 9.08 mM) and dimethyl acetylenedicarboxylate (1.40 g, 9.82 mM) in t-butanol (20 mL) was refluxed fpr 18 hr under a nitrogen atmosphere. The reaction mixture was cooled to room temperature and potassium t-butoxide (1.10 g, 9.82 mM) was added in one portion whereupon a precipitate formed. After refluxing this mixture for 1.5 hr, it was cooled to room temperature and filtered to separate the solids. The solids were dissolved in water and the resulting solution acidified with 1N H2SO4 to form a precipitate. The mixture was filtered and the collected solids were washed with water and dried to give the title compound (1.66 g, 66.4%) as a tan solid. An analytical sample of this material was obtained by recrystallization of a portion from ethyl acetate/hexane to give off white crystals, mp 167°-168° C.; MS(CI): 276 (M+H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05733910uspto-grants-1998_03