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Methyl 2-bromo-3-(4-fluorophenyl)propanoate → Methyl 3-(4-fluorophenyl)propanoate

HRID 647430
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 647430
Br[CH:2]([CH2:7][C:8]1[CH:13]=[CH:12][C:11]([F:14])=[CH:10][CH:9]=1)[C:3]([O:5][CH3:6])=[O:4]>C(O)(=O)C.[Zn]>[F:14][C:11]1[CH:10]=[CH:9][C:8]([CH2:7][CH2:2][C:3]([O:5][CH3:6])=[O:4])=[CH:13][CH:12]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 1

HCID 12188683Methyl 2-bromo-3-(4-fluorophenyl)propanoate

Produkt 1

HCID 22906572Methyl 3-(4-fluorophenyl)propanoate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23994ZincKatalysatorHCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

Crude methyl 2-bromo-3-(4-fluorophenyl)propionate in acetic acid (330 ml) was stirred and treated with zinc dust (32.75 g) in portions over 30 minutes. The mixture was stirred for an additional 30 minutes and filtered, and the filter cake was washed with acetic acid. After the filtrate was evaporated the residue was partitioned between methylene chloride and water to give crude methyl 3-(4-fluorophenyl)propionate, which was refluxed with aqueous sodium hydroxide (400 ml, 10%) for 2 hrs, cooled, treated with decolorizing carbon, and filtered. The filtrate was acidified with 5 N HCl and filtered. The filter cake was washed extensively with water to give 3-(4-fluorophenyl)propionic acid (20.0 g) as colourless crystals, mp 90° C.

Aufarbeitung

  1. filtrationfiltered
  2. washthe filter cake was washed with acetic acid
  3. customAfter the filtrate was evaporated the residue
  4. customwas partitioned between methylene chloride and water

Quellen und Nachweise

ORD-Eintrag
ord-d68543213f61443bad84c49c21c173eb
Quelldatensatz
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04409017

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