Reaktion #1946699

ord-a9d8c5ab1837485797585a367ad4c303

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe title compound was prepared
  2. 2
    SonstigeThe crude product was chromatographed on silica gel
  3. 3
    Wascheneluting with 2:1 hexane

Vorschrift

The title compound was prepared as described in General Method 3 using 1.73 g (8.86 mmol) of 4-methyl-1-(4-methyl-thiazol-5-yl)-pent-1-en-3-one (prepared in Example B-1) and 0.4 g of 5% Pd/BaSO4 in THF:MeOH (25 mL:25 mL). The crude product was chromatographed on silica gel, eluting with 2:1 hexane:EtOAc, to give the title compound. 1H NMR (CDCl3): δ1.03 (d, 6 H), 2.35 (s, 3 H), 2.49-2.56 (m, 1 H), 2.72 (t, 2 H), 2.98 (t, 2 H), 8.49 (s, 1 H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06528510B1uspto-grants-2003_03