Ammonium Chloride → Diethyl 5-ethylpyridine-2,3-dicarboxylate

HRID 54176

Reaktionsgleichung

Reaktionsgleichung von HRID 54176
C(O[CH:4]=[C:5]([C:11]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=O)[C:6]([O:8][CH2:9][CH3:10])=[O:7])C.O1CC[N:21]([CH:24]=[CH:25][CH2:26][CH3:27])CC1.[NH4+].[Cl-]>CO.C(O)(=O)C>[CH2:26]([C:25]1[CH:4]=[C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])[C:11]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[N:21][CH:24]=1)[CH3:27]

Komponenten

6

Versuchsvorschrift

To a solution of diethyl ethoxymethyleneoxalacetate (43.2 g, 0.16 mol) dissolved in CH3OH (150 mL) at -10° under N2 is added 1-morpholinobutene (25 g, 0.16 mol). The reaction is slowly warmed to room temperature over three hours, after which the CH3OH is removed in vacuo. The residue is dissolved in acetic acid (100 mL) and this solution slowly added to NH4Cl (34.2 g, 0.64 mol) dissolved in acetic acid (200 mL) at 50°-70°. The reaction is then heated to 90°-95° for two hours and 30 minutes, concentrated in vacuo, partitioned between water and the CH2Cl2, and the organic phase chromatographed over silica gel with CH2Cl2 --CH3CN (95:5) elution to give the product as an oil. Distillation at 123°-155° at 0.15 mm gives the product (23.4 g, 83% pure, 55%).

Aufarbeitung

  1. customafter which the CH3OH is removed in vacuo
  2. dissolutionThe residue is dissolved in acetic acid (100 mL)
  3. temperatureThe reaction is then heated to 90°-95° for two hours and 30 minutes
  4. concentrationconcentrated in vacuo
  5. custompartitioned between water
  6. customthe CH2Cl2, and the organic phase chromatographed over silica gel with CH2Cl2 --CH3CN (95:5) elution

Quellen und Nachweise

ORD-Eintrag
ord-0b89315e3a1347fdb5e029a78e591590
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05622913

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