Dimethyl acetylenedicarboxylate → HCID 178418266, Verbindung

HRID 3115

Reaktionsgleichung

Reaktionsgleichung von HRID 3115
[NH2:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]([O:12][CH3:13])[C:3]=1[C:4]([O:6]C)=O.[C:14]([C:20]([O:22][CH3:23])=[O:21])#[C:15][C:16]([O:18][CH3:19])=[O:17].CC(C)([O-])C.[K+]>C(O)(C)(C)C>[OH:6][C:4]1[C:3]2[C:2](=[CH:11][CH:10]=[CH:9][C:8]=2[O:12][CH3:13])[N:1]=[C:15]([C:16]([O:18][CH3:19])=[O:17])[C:14]=1[C:20]([O:22][CH3:23])=[O:21]

Komponenten

5

Versuchsvorschrift

A solution of methyl 2-amino-6-methoxybenzoate ((1.30 g, 7.17 mM) and dimethyl acetylenedicarboxylate (1.17 g, 8.23 mM) in t-butanol (11 mL) was refluxed under a nitrogen atmosphere for 4 hr. The reaction mixture was cooled to room temperature, potassium t-butoxide (0.92 g, 8.23 mM) was added, and the resulting mixture was heated to 90° C. for 1.5 hr during which solids precipitated out of solution. The mixture was cooled to room temperature, filtered and the collected solids were dissolved in water. The resulting solution was acidified with 1N H2SO4 to form a light tan precipitate. The solids were collected, filtered, washed with water and air dried to provide the desired compound (1.35 g, 65%) as a tan solid. A 0.28 g portion of this material was recrystallized from ethyl acetate to provide an analytical sample (0.24 g) of the title compound as a white solid, mp 184°-186° C.; MS(CI): 292 (M+H).

Aufarbeitung

  1. temperaturethe resulting mixture was heated to 90° C. for 1.5 hr during which solids
  2. customprecipitated out of solution
  3. temperatureThe mixture was cooled to room temperature
  4. filtrationfiltered
  5. dissolutionthe collected solids were dissolved in water
  6. customto form a light tan precipitate
  7. customThe solids were collected
  8. filtrationfiltered
  9. washwashed with water and air
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-1239a307ee3d4a5296ffa6fb6b34bcfc
Quelldatensatz
uspto-grants-1998_03
Patentnummer
US05733910

Verknüpfte Notizen

Wird geladen…