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Potassium Carbonate → Acetic acid, 2-(2-acetyl-4-methoxyphenoxy)-

HRID 2091177
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2091177
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[C:10](=[O:12])[CH3:11].Br[CH2:14][C:15]([O:17]C)=[O:16].C(=O)([O-])[O-].[K+].[K+].[OH-].[Na+]>C(O)C.O1CCCC1.CN(C)C=O>[C:10]([C:3]1[CH:4]=[C:5]([O:8][CH3:9])[CH:6]=[CH:7][C:2]=1[O:1][CH2:14][C:15]([OH:17])=[O:16])(=[O:12])[CH3:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 11430Potassium CarbonateHCID 14798Sodium HydroxideHCID 60984Methyl bromoacetateHCID 697141-(2-Hydroxy-5-methoxyphenyl)ethan-1-one

Produkt 1

HCID 13156994Acetic acid, 2-(2-acetyl-4-methoxyphenoxy)-

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 702
Ethanol
Lösungsmittel
HCID 6228DimethylformamideLösungsmittel
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a mixture of 1-(2-hydroxy-5-methoxyphenyl)ethanone (25.0 g), methyl bromoacetate (15.5 mL) and N,N-dimethylformamide (250 mL) was added potassium carbonate (31.1 g), and the mixture was stirred overnight at room temperature. The insoluble material was filtered off, 1N hydrochloric acid was added to the filtrate, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give a brown solid. To a mixture of the obtained solid, tetrahydrofuran (300 mL) and ethanol (300 mL) was added 1N aqueous sodium hydroxide solution (300 mL), and the mixture was stirred overnight at room temperature, and concentrated under reduced pressure. 1N Hydrochloric acid (300 mL) was added to the residue at 0° C., and the resulting precipitate was collected by filtration to give the title object compound (34.2 g, quantitative) as a white solid.

Aufarbeitung

  1. filtrationThe insoluble material was filtered off
  2. addition1N hydrochloric acid was added to the filtrate
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe extract was washed with saturated brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customto give a brown solid
  8. stirringthe mixture was stirred overnight at room temperature
  9. concentrationconcentrated under reduced pressure
  10. addition1N Hydrochloric acid (300 mL) was added to the residue at 0° C.
  11. filtrationthe resulting precipitate was collected by filtration
  12. customto give the title object compound (34.2 g, quantitative) as a white solid

Quellen und Nachweise

ORD-Eintrag
ord-a48619a13d034998aa4c0e0937fc3fd3
Quelldatensatz
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08436043B2

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