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4-Bromo-3-fluoro-N-methoxy-N-methylbenzamide → 1-(4-Bromo-3-fluorophenyl)butan-1-one

HRID 394889
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Reaktionsgleichung

Reaktionsgleichung von HRID 394889
[Br:1][C:2]1[CH:13]=[CH:12][C:5]([C:6](N(OC)C)=[O:7])=[CH:4][C:3]=1[F:14].[CH2:15]([Mg]Br)[CH2:16][CH3:17]>O1CCCC1>[Br:1][C:2]1[CH:13]=[CH:12][C:5]([C:6](=[O:7])[CH2:15][CH2:16][CH3:17])=[CH:4][C:3]=1[F:14]
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Komponenten

4

Edukt 2

HCID 223138234-Bromo-3-fluoro-N-methoxy-N-methylbenzamideHCID 178455851HCID 178455851, Verbindung

Produkt 1

HCID 223138401-(4-Bromo-3-fluorophenyl)butan-1-oneAusbeute 81,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a stirred solution of 4-Bromo-3-fluoro-N-methoxy-N-methylbenzamide (3.0 g, 12.19 mmol) in tetrahydrofuran (35 ml) was added 2M n-propylmagnesium bromide (12.2 ml, 24.38 mmol) dropwise under nitrogen at 0° C. The reaction mixture was stirred at room temperature for 2 h. This was quenched by sat. ammonium chloride and stirred at rt for 30 min. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The extracts was dried (MgSO4) and concentrated. This was purified on silica gel eluting with ethyl acetate/hexane (1:10) to afford 2.44 g (81.7%) of the titled compound as a slight yellow oil.

Aufarbeitung

  1. customThis was quenched by sat. ammonium chloride
  2. stirringstirred at rt for 30 min
  3. customThe organic layer was separated
  4. extractionthe aqueous layer was extracted with ethyl acetate
  5. dry with materialThe extracts was dried (MgSO4)
  6. concentrationconcentrated
  7. customThis was purified on silica gel eluting with ethyl acetate/hexane (1:10)

Quellen und Nachweise

ORD-Eintrag
ord-ba47e843e9114b0ea614bbaad30cd6a2
Quelldatensatz
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06603008B1

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