Sodium Hydroxide → 3-[2,4-Dimethoxy-5-(4-methoxybenzoyl)phenyl]propionic acid

HRID 893418Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 893418
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[C:6]([C:11](=[O:20])[C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=2)=[CH:5][C:4]=1[CH2:21][CH2:22][C:23]([O:25]C)=[O:24].[OH-].[Na+]>O1CCOCC1>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[C:6]([C:11](=[O:20])[C:12]2[CH:13]=[CH:14][C:15]([O:18][CH3:19])=[CH:16][CH:17]=2)=[CH:5][C:4]=1[CH2:21][CH2:22][C:23]([OH:25])=[O:24]

Komponenten

4

Versuchsvorschrift

60.9 g of methyl 3-[2,4-dimethoxy-5-(4-methoxybenzoyl)phenyl]propionate are mixed with 300 ml of 2N sodium hydroxide solution and 300 ml of dioxane and stirred overnight. The dioxane is then removed in vacuo, and the alkaline aqueous solution is extracted once with 100 ml of ethyl acetate. The aqueous phase is adjusted to pH 2 with concentrated hydrochloric acid, when part of the product separates out. The mixture is extracted three times with 200 ml of ethyl acetate each time, and the organic phase is washed with water, dried over sodium sulfate and concentrated. The residue is recrystallized from ethyl acetate/acetone/hexane.

Aufarbeitung

  1. customThe dioxane is then removed in vacuo
  2. extractionthe alkaline aqueous solution is extracted once with 100 ml of ethyl acetate
  3. extractionThe mixture is extracted three times with 200 ml of ethyl acetate each time
  4. washthe organic phase is washed with water
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated
  7. customThe residue is recrystallized from ethyl acetate/acetone/hexane

Quellen und Nachweise

ORD-Eintrag
ord-c243e0a9001f4ea59539d42c52d1062f
Quelldatensatz
uspto-grants-1992_06
Patentnummer
US05124478

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