Reaktion #1144435

ord-536f8196f59441eb9dc123a8eaaba2eb

Reaktionsgleichung

CCc1c[nH]c(=O)[nH]c1=O
5-ethyluracil
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCCCn1cc(CC)c(=O)[nH]c1=O
1-butyl-5-ethyluracil
Ausbeute 69.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
120°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe reaction mixture was concentrated under reduced pressure
  2. 2
    Einengenthe organic layer was concentrated under reduced pressure
  3. 3
    Wascheneluted with 30% ethyl acetate/hexane

Vorschrift

To a solution of 5.6 g (40 mmol) of 5-ethyluracil in 60 ml of dimethylformamide, 5.5 g (40 mmol) of potassium carbonate and 2.3 ml (20 mmol) of n-iodobutane were added and stirred for 2 hours at 120° C. The reaction mixture was concentrated under reduced pressure and distributed between dichloromethane and aqueous solution of ammonium chloride, and the organic layer was concentrated under reduced pressure. The residue was adsorbed on a silica gel column and eluted with 30% ethyl acetate/hexane to obtain 2.7 g of 1-butyl-5-ethyluracil (Yield: 69%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE037979E1uspto-grants-2003_02