Sodium Hydroxide → 2-(4-Methoxy-3-propoxyphenyl)-4-(5-carbonyl-2-furyl)thiazole

HRID 1596429Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1596429
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[S:10][CH:11]=[C:12]([C:14]3[O:15][C:16]([C:19](OC)=[O:20])=[CH:17][CH:18]=3)[N:13]=2)=[CH:5][C:4]=1[O:23][CH2:24][CH2:25][CH3:26].O1CCOCC1.[OH-].[Na+]>CO>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[S:10][CH:11]=[C:12]([CH:14]3[CH:18]=[CH:17][C:16](=[C:19]=[O:20])[O:15]3)[N:13]=2)=[CH:5][C:4]=1[O:23][CH2:24][CH2:25][CH3:26]

Komponenten

5

Edukt 3

HCID 14798Sodium HydroxideHCID 312751,4-DioxaneHCID 185116982-(4-Methoxy-3-propoxyphenyl)-4-(5-methoxycarbonyl-2-furyl)thiazole

Produkt 1

HCID 865842582-(4-Methoxy-3-propoxyphenyl)-4-(5-carbonyl-2-furyl)thiazoleAusbeute 47,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a suspension of 970 mg of 2-(4-methoxy-3-propoxyphenyl)-4-(5-methoxycarbonyl-2-furyl)thiazole in 30 ml of methanol was added 20 ml of 1,4-dioxane and 5 ml of a 5 N aqueous sodium hydroxide solution. The reaction mixture was refluxed for 3 hours, then concentrated approximately {fraction (1/10)}. Water was added to the residue, and washed with ethyl acetate. To the aqueous layer was acidified with 5 N hydrochloric acid, and extracted with ethyl acetate. The combined organic layer was washed with water and a saturated aqueous sodium chloride solution, and dried with magnesium sulfate. Evaporation the solution, the residue was recrystallized from ethyl acetate to obtain 420 mg of 2-(4-methoxy-3-propoxyphenyl)-4-(5-carbonyl-2-furyl)thiazole as a white powder. mp. 191.0-192.0° C.

Aufarbeitung

  1. temperatureThe reaction mixture was refluxed for 3 hours
  2. concentrationconcentrated approximately {fraction (1/10)}
  3. additionWater was added to the residue
  4. washwashed with ethyl acetate
  5. extractionextracted with ethyl acetate
  6. washThe combined organic layer was washed with water
  7. dry with materiala saturated aqueous sodium chloride solution, and dried with magnesium sulfate
  8. customEvaporation the solution
  9. customthe residue was recrystallized from ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-9e1454c018cd4637add61a77cab59b3d
Quelldatensatz
uspto-grants-2001_09
Patentnummer
US06291487B1

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