Reaktion #336751

ord-7535c6cada5e4d8aa4c298bdb54a4fc2

Reaktionsgleichung

O=C(CCCCl)[c-]1cccc1.[Fe+2].c1cc[cH-]c1
4-chlorobutyroylferrocene
[Fe+2].c1cc[cH-]c1.c1cc[cH-]c1
ferrocene
O=C(CCCCl)[c-]1cccc1.O=C(CCCCl)[c-]1cccc1.[Fe+2]
1,1'-di(4-chlorobutyroyl)ferrocene
[Cl][Sn][Cl]
SnCl2
O=C(CCCCl)[c-]1cccc1.[Fe+2].c1cc[cH-]c1
4-chlorobutyroylferrocene
[Fe+2].c1cc[cH-]c1.c1cc[cH-]c1
ferrocene
O=C(Cl)CCCCl
4-chlorobutyryl chloride

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONare introduced into the glass beaker
  2. 2
    workup.ADDITIONare then poured in

Vorschrift

In an inert atmosphere, 170 mg of PtO2.xH2O (containing 80% of Pt) and 5 mg of anhydrous SnCl2 are introduced into the glass beaker. 120 cm3 of glacial acetic acid and 29.1 g (0.10 mol) of 4-chlorobutyroylferrocene whose main impurities are 1.4% by weight of ferrocene and 0.88% by weight of 1,1'-di(4-chlorobutyroyl)ferrocene are then poured in. This 4-chlorobutyroylferrocene was obtained in the customary manner by a reaction of the Friedel-Crafts type between ferrocene and 4-chlorobutyryl chloride in CH2Cl2 in the presence of AlCl3 as catalyst, followed by recrystallisation of the crude product obtained from hexane.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05214175uspto-grants-1993_05