Dimethyl acetylenedicarboxylate → HCID 178418285, Verbindung

HRID 3106

Reaktionsgleichung

Reaktionsgleichung von HRID 3106
[NH2:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]([CH3:12])[C:3]=1[C:4]([O:6]C)=O.[C:13]([C:19]([O:21][CH3:22])=[O:20])#[C:14][C:15]([O:17][CH3:18])=[O:16].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[CH3:12])[N:1]=[C:14]([C:15]([O:17][CH3:18])=[O:16])[C:13]=1[C:19]([O:21][CH3:22])=[O:20]

Komponenten

5

Versuchsvorschrift

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).

Aufarbeitung

  1. temperaturewas refluxed fpr 18 hr under a nitrogen atmosphere
  2. customformed
  3. temperatureAfter refluxing this mixture for 1.5 hr
  4. temperatureit was cooled to room temperature
  5. filtrationfiltered
  6. customto separate the solids
  7. dissolutionThe solids were dissolved in water
  8. customto form a precipitate
  9. filtrationThe mixture was filtered
  10. washthe collected solids were washed with water
  11. customdried

Quellen und Nachweise

ORD-Eintrag
ord-3dda300c17224ab9a94f5d53c331760a
Quelldatensatz
uspto-grants-1998_03
Patentnummer
US05733910

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