Potassium Iodide → 3-Methoxy-4-(3-morpholinopropoxy)benzoic acid

HRID 1596272Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1596272
[OH:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[O:11][CH3:12].[O:13]1[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][CH2:21]Cl)[CH2:15][CH2:14]1.C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>CN(C=O)C>[CH3:12][O:11][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:2]=1[O:1][CH2:21][CH2:20][CH2:19][N:16]1[CH2:17][CH2:18][O:13][CH2:14][CH2:15]1)[C:6]([OH:8])=[O:7]

Komponenten

6

Edukt 4

HCID 4875Potassium IodideHCID 8468Vanillic AcidHCID 11430Potassium CarbonateHCID 958344-(3-Chloropropyl)morpholine

Produkt 1

HCID 216992843-Methoxy-4-(3-morpholinopropoxy)benzoic acidAusbeute 109,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A mixture of 4-hydroxy-3-methoxybenzoic acid (4.5 g, 26.8 mmol), 3-morpholinopropyl chloride (9.5 g, 58.0 mmol), (prepared according to J. Am. Chem. Soc. 1945, 67, 736), potassium carbonate (8.0 g, 58 mmol), potassium iodide (1.0 g, 0.22 mmol) and DMF (80 ml) was stirred and heated at 100° C. for 3 hours. The solid was removed by filtration and the filtrate evaporated. The residue was dissolved in ethanol (50 ml), 2 M sodium hydroxide (50 ml) was added and the mixture heated at 90° C. for 2 hours. After partial evaporation, the mixture was acidified with concentrated hydrochloric acid, washed with ether and then subjected to purification on a Diaion (trade mark of Mitsubishi) HP20SS resin column, eluting with water and then with a gradient of methanol (0 to 25%) in hydrochloric acid (pH2). Partial evaporation of the solvents and lyophilisation gave 3-methoxy-4-(3-morpholinopropoxy)benzoic acid (8.65 g, 97%).

Aufarbeitung

  1. customThe solid was removed by filtration
  2. customthe filtrate evaporated
  3. dissolutionThe residue was dissolved in ethanol (50 ml)
  4. addition2 M sodium hydroxide (50 ml) was added
  5. temperaturethe mixture heated at 90° C. for 2 hours
  6. customAfter partial evaporation
  7. washwashed with ether
  8. customsubjected to purification on a Diaion (trade mark of Mitsubishi) HP20SS resin column
  9. washeluting with water
  10. customPartial evaporation of the solvents and lyophilisation

Quellen und Nachweise

ORD-Eintrag
ord-0bd8b8ccd2ed408994779b03ef386f85
Quelldatensatz
uspto-grants-2001_09
Patentnummer
US06291455B1

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