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Thionyl Chloride → HCID 53703120, Verbindung

HRID 1731165
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1731165
[Cl:1][C:2]1[CH:22]=[CH:21][C:5]([C:6]([C:8]2[C:9]([CH3:20])=[C:10]([CH2:14][CH2:15][CH2:16][C:17](O)=[O:18])[CH:11]=[CH:12][CH:13]=2)=[O:7])=[CH:4][CH:3]=1.S(Cl)([Cl:25])=O>>[Cl:1][C:2]1[CH:22]=[CH:21][C:5]([C:6]([C:8]2[C:9]([CH3:20])=[C:10]([CH2:14][CH2:15][CH2:16][C:17]([Cl:25])=[O:18])[CH:11]=[CH:12][CH:13]=2)=[O:7])=[CH:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 24386Thionyl ChlorideHCID 1910664-(2-Methyl-3-(4-chlorobenzoyl)phenyl)butanoic acid

Produkt 1

HCID 53703120HCID 53703120, Verbindung

Versuchsvorschrift

A mixture of 8 g of 4-(3'-p-chlorobenzoyl-2'-methylphenyl)-butyric acid (Example V) and 80 ml of thionyl chloride was refluxed for 45 minutes and after removal of excess thionyl chloride under reduced pressure, 60 ml of benzene were added thereto. The traces of thionyl chloride were removed by entrainment with benzene. This operation was repeated 3 times. The residue was taken up in tetra-hydrofuran to obtain a solution of 4-(3'-p-chlorobenzoyl-2'-methyl-phenyl)-butyric acid chloride which was used as is for the next step.

Aufarbeitung

  1. temperaturewas refluxed for 45 minutes
  2. customafter removal of excess thionyl chloride under reduced pressure, 60 ml of benzene
addition
were added
  • customThe traces of thionyl chloride were removed by entrainment with benzene
  • Quellen und Nachweise

    ORD-Eintrag
    ord-ca47c8853acb4e5fb2ad2d9f6644718c
    Quelldatensatz
    uspto-grants-1976_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US03995056

    Notizen zur Reaktion

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