Pyridine → Methyl 3-pentanamidobenzoate

HRID 2732

Reaktionsgleichung

Reaktionsgleichung von HRID 2732
N1C=CC=CC=1.[NH2:7][C:8]1[CH:9]=[C:10]([CH:15]=[CH:16][CH:17]=1)[C:11]([O:13][CH3:14])=[O:12].[C:18](Cl)(=[O:23])[CH2:19][CH2:20][CH2:21][CH3:22]>O>[C:18]([NH:7][C:8]1[CH:9]=[C:10]([CH:15]=[CH:16][CH:17]=1)[C:11]([O:13][CH3:14])=[O:12])(=[O:23])[CH2:19][CH2:20][CH2:21][CH3:22]

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 61186Valeryl chlorideHCID 78274Benzoic acid, 3-amino-, methyl ester

Produkt 1

HCID 19171455Methyl 3-pentanamidobenzoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

To anhydrous pyridine (120 ml), methyl 3-aminobenzoate (5.00 g) was dissolved, and valeryl chloride (4.13 ml) was added while cooling on ice. The mixture was stirred at room temperature for 4 hours. Distilled water was added to the solution. The whole was extracted with ethyl acetate, washed with 5% sodium hydrogencarbonate aqueous solution and water, and dried over anhydrous sodium sulfate. The solvent was evaporated, and the residue was purified by silica gel column chromatography (Kieselgel 60=170 g, hexane/ethyl acetate=3/1) to obtain the above-captioned compound ([6]-(62)-90) (7.70 g) as a white solid.

Aufarbeitung

  1. temperaturewhile cooling on ice
  2. extractionThe whole was extracted with ethyl acetate
  3. washwashed with 5% sodium hydrogencarbonate aqueous solution and water
  4. dry with materialdried over anhydrous sodium sulfate
  5. customThe solvent was evaporated
  6. customthe residue was purified by silica gel column chromatography (Kieselgel 60=170 g, hexane/ethyl acetate=3/1)
  7. customto obtain the above-captioned compound ([6]-(62)-90) (7.70 g) as a white solid

Quellen und Nachweise

ORD-Eintrag
ord-afe1acea3c9c4770b2b372a33f6672d6
Quelldatensatz
uspto-grants-1998_03
Patentnummer
US05731310

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