Water → Ethyl 2-(3-fluorophenoxy)-2-methylpropanoate

HRID 56274

Reaktionsgleichung

Reaktionsgleichung von HRID 56274
[F:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.Br[C:10]([CH3:17])([CH3:16])[C:11]([O:13][CH2:14][CH3:15])=[O:12].C([O-])([O-])=O.[K+].[K+].O>CC(C)=O>[F:1][C:2]1[CH:3]=[C:4]([CH:5]=[CH:6][CH:7]=1)[O:8][C:10]([CH3:17])([CH3:16])[C:11]([O:13][CH2:14][CH3:15])=[O:12]

Komponenten

6

Edukt 4

HCID 962WaterHCID 97433-FluorophenolHCID 11430Potassium CarbonateHCID 11745Propanoic acid, 2-bromo-2-methyl-, ethyl ester

Produkt 1

HCID 58243746Ethyl 2-(3-fluorophenoxy)-2-methylpropanoateAusbeute 47,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel

Versuchsvorschrift

A mixture of 3-fluorophenol (3.36 g, 30.0 mmol), ethyl 2-bromo-2-methylpropanoate (8.78 g, 45.0 mmol) and K2CO3 (6.22 g, 45.0 mmol) in acetone (50 mL) was refluxed overnight. The mixture was cooled to rt and 60 mL of water was added. The resulting mixture was extracted with DCM (40 mL×2). The combined organic phases were washed with brine (40 mL×2), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=4:1) to give the title compound as colorless liquid (3.20 g, 47%).

Aufarbeitung

  1. temperaturewas refluxed overnight
  2. extractionThe resulting mixture was extracted with DCM (40 mL×2)
  3. washThe combined organic phases were washed with brine (40 mL×2)
  4. dry with materialdried over anhydrous Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=4:1)

Quellen und Nachweise

ORD-Eintrag
ord-aa565b51f54e4f788b914aab720434e4
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09434695B2

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