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Carbon Dioxide → 2,3-Difluoro-6-(2-methoxyethoxy)benzoic acid

HRID 1968592
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1968592
[F:1][C:2]1[CH:3]=[C:4]([O:9][CH2:10][CH2:11][O:12][CH3:13])[CH:5]=[CH:6][C:7]=1[F:8].C([Li])CCC.[C:19](=[O:21])=[O:20].Cl>O1CCCC1>[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[C:4]([O:9][CH2:10][CH2:11][O:12][CH3:13])[C:3]=1[C:19]([OH:21])=[O:20]
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Komponenten

6

Edukt 4

HCID 280Carbon DioxideHCID 313Hydrochloric AcidHCID 574290663,4-Difluoro-1-(2-methoxyethoxy)benzeneHCID 178418339Butyllithium

Produkt 1

HCID 574290652,3-Difluoro-6-(2-methoxyethoxy)benzoic acidAusbeute 81,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028
Tetrahydrofuran
Lösungsmittel

Versuchsvorschrift

To a suspension of 3,4-difluorophenol (2 g) and cesium carbonate (7.51 g) in N,N-dimethylformamide (15 mL) was added 2-methoxyethyl bromide (2.14 g), and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water, and the resulting mixture was extracted with diethyl ether. The extract was washed with water twice and brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=5/1) to give 3,4-difluoro-1-(2-methoxyethoxy)-benzene (2.49 g). To the solution of the obtained 3,4-difluoro-1-(2-methoxyethoxy)benzene (1.47 g) in tetrahydrofuran (39 mL) was added n-butyllithium (2.64 mol/L n-hexane solution, 3.25 mL) at −78° C., and the mixture was stirred at the same temperature for 30 minutes. To the reaction mixture was added dry ice (10 g), and the mixture was stirred at the same temperature for 30 minutes, and then stirred at room temperature for 30 minutes. To the reaction mixture was added 2 mol/L hydrochloric acid, and the resulting mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to give the title compound (1.48 g).

Aufarbeitung

  1. stirringthe mixture was stirred at the same temperature for 30 minutes
  2. stirringstirred at room temperature for 30 minutes
  3. extractionthe resulting mixture was extracted with ethyl acetate
  4. washThe extract was washed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customThe solvent was removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-f5d36e6d2e3548d69d0f072e75a81db9
Quelldatensatz
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08426427B2

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