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2-(4-Fluorophenyl)acetic acid → 4-Fluorophenylacetyl chloride

HRID 31150
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 31150
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([OH:11])=O)=[CH:4][CH:3]=1.S(Cl)([Cl:14])=O>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([Cl:14])=[O:11])=[CH:4][CH:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 98372-(4-Fluorophenyl)acetic acid2×HCID 24386Thionyl Chloride

Produkt 1

HCID 37449884-Fluorophenylacetyl chloride

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

4-Fluorophenylacetic acid [starting compound B] (15 g) was dissolved in thionyl chloride (15 ml) to prepare a solution which was then heated at 60° C. for one hr. Excess thionyl chloride was removed by evaporation under the reduced pressure to give 4-fluorophenylacetyl chloride. The acid chloride was dissolved in acetone (200 ml). Ammonium acetate (112 g) was added to the solution, and the mixture was stirred at room temperature for 17 hr. An aqueous saturated sodium hydrogencarbonate solution (150 ml) was added thereto, and the mixture was stirred at room temperature for one hr. The reaction solution was then extracted with chloroform, and the solvent in the extract was removed by evaporation to give a crude crystal. The resultant crude crystal was washed with a hexane/ethyl acetate (2/1) mixed solution to give 4-fluorophenylacetamide (10.5 g, yield 70%).

Aufarbeitung

  1. customto prepare a solution which
  2. customExcess thionyl chloride was removed by evaporation under the reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-8b889680510b4a0da9efcc345408252a
Quelldatensatz
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07425564B2

Notizen zur Reaktion

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