Methoxyacetyl chloride → Ethyl 2,4-bis(methoxyacetylamino)benzoate

HRID 1165882Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1165882
[NH2:1][C:2]1[CH:12]=[C:11]([NH2:13])[CH:10]=[CH:9][C:3]=1[C:4]([O:6][CH2:7][CH3:8])=[O:5].[CH3:14][O:15][CH2:16][C:17](Cl)=[O:18]>N1C=CC=CC=1>[CH3:14][O:15][CH2:16][C:17]([NH:1][C:2]1[CH:12]=[C:11]([NH:13][C:17](=[O:18])[CH2:16][O:15][CH3:14])[CH:10]=[CH:9][C:3]=1[C:4]([O:6][CH2:7][CH3:8])=[O:5])=[O:18]

Komponenten

4

Versuchsvorschrift

To a solution of ethyl 2,4-diaminobenzoate (3.6 g) in pyridine (80 ml) is added dropwise methoxyacetyl chloride (4.0 ml) at room temperature. The mixture is stirred at room temperature for 3 hours, and thereafter, pyridine is distilled off under reduced pressure. To the residue are added water and chloroform. The organic layer is separated and washed with water and then with aqueous saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent is distilled off under reduced pressure, and the resulting oily substance is dissolved in ethyl acetate-hexane, and the solution is allowed to stand at -30° C. for 6 hours. The precipitated crystals are separated by filtration to give the title compound (6.0 g) having the following physical properties.

Aufarbeitung

  1. distillationpyridine is distilled off under reduced pressure
  2. additionTo the residue are added water and chloroform
  3. customThe organic layer is separated
  4. washwashed with water
  5. dry with materialwith aqueous saturated sodium chloride solution, and dried over anhydrous sodium sulfate
  6. distillationThe solvent is distilled off under reduced pressure
  7. dissolutionthe resulting oily substance is dissolved in ethyl acetate-hexane
  8. waitto stand at -30° C. for 6 hours
  9. customThe precipitated crystals are separated by filtration

Quellen und Nachweise

ORD-Eintrag
ord-c2dba8e770cd4b999a6d31eea55abdc8
Quelldatensatz
uspto-grants-1990_03
Patentnummer
US04912135

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