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Triethylamine → 5-Bromo-2-(4-fluoro-phenoxymethyl)-pyridine

HRID 77993
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 77993
[F:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[H-].[Na+].Cl.[Br:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:19]Cl)=[N:17][CH:18]=1.C(N(CC)CC)C>C(OCC)(=O)C.O.CN(C)C=O>[Br:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:19][O:8][C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=2)=[N:17][CH:18]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 8471TriethylamineHCID 97324-FluorophenolHCID 24758Sodium hydrideHCID 534382005-Bromo-2-(chloromethyl)pyridine hydrochloride

Produkt 1

HCID 592552365-Bromo-2-(4-fluoro-phenoxymethyl)-pyridineAusbeute 63,6 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962
Water
Lösungsmittel
HCID 6228DimethylformamideLösungsmittel
HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

To an N,N-dimethylformamide (40.0 mL) solution of 4-fluorophenol (3.00 g, 26.8 mmol) was added sodium hydride (1.00 g, 25.0 mmol, 60% in oil) on an ice bath (0° C.) under nitrogen atmosphere, which was stirred for 20 minutes at room temperature. To the reaction solution was then added a mixture of 5-bromo-2-chloromethyl-pyridine hydrochloride (4.6 g, 22.3 mmol) described in Manufacturing Example 54-1-2 and triethylamine (30.6 mL, 20.4 mmol), which was stirred for 10 minutes at room temperature. Water and ethyl acetate were added to the reaction mixture, and the organic layer was extracted with ethyl acetate. This organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The solvent was evaporated from the filtrate under a reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:4) to obtain the title compound (4.0 g, 63.6%).

Aufarbeitung

  1. additionTo the reaction solution was then added
  2. stirringwas stirred for 10 minutes at room temperature
  3. extractionthe organic layer was extracted with ethyl acetate
  4. washThis organic layer was washed with water and saturated aqueous sodium chloride
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customThe solvent was evaporated from the filtrate under a reduced pressure
  8. customthe residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:4)

Quellen und Nachweise

ORD-Eintrag
ord-7c71563111e545da838ab2302ab4d6a1
Quelldatensatz
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08841327B2

Notizen zur Reaktion

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