Reaktion #463778

ord-e5864c8f3b0946adbdba3f81e27aa45c

Reaktionsgleichung

COC(=O)c1ccc(CCl)o1
methyl 5-chloromethyl-2-furoate
COC(=O)c1ccc(C)o1
title compound
Ausbeute 94.0%
COC(=O)c1ccc(C)o1
Methyl 5-methyl-2-furoate
Ausbeute 94.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe catalyst was filtered off
  2. 2
    Waschenwashed with ethyl acetate
  3. 3
    EinengenThe combined filtrates were concentrated in vacuo
  4. 4
    Sonstigethe residue purified by chromatography on silica gel eluting with 10% ethyl acetate in hexane

Vorschrift

A solution of methyl 5-chloromethyl-2-furoate (5.0g, 28.7mmol) in ethyl acetate (40ml) was hydrogenated over 10% palladium on charcoal (50mg) for 3h. The catalyst was filtered off and washed with ethyl acetate. The combined filtrates were concentrated in vacuo and the residue purified by chromatography on silica gel eluting with 10% ethyl acetate in hexane to yield the title compound as a colourless oil (3.78g, 94%); vmax (CH2Cl2) 1725, 1534, 1522, 1437 and 1311cm-1 ; δH (CDCl3, 90MHz) 2.38 (3H, s), 3.86 (3H, s), 6.12 (1H, br d, J 4Hz) and 7.07 (1H, d, J 4Hz). [Mass spectrum: M+(140)].

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06020329uspto-grants-2000_02