Réaction #5812

ord-2c45a2c2970649979f6c2d88874662a4

Équation de réaction

O=Cc1ccc(F)cc1
4-fluorobenzaldehyde
C=CC(=O)CC
ethyl vinyl ketone
CCN(CC)CC
triethylamine
CCC(=O)CCC(=O)c1ccc(F)cc1
1-(4-fluorophenyl)-1,4-hexanedione
Rendement 89.5%

Solvants

Conditions de réaction

Température
70°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavagewashed with 2×300 mL of water, 2×100 mL of 2M hydrochloric acid, 100 mL of water, 200 mL of a saturated solution of sodium bicarbonate and brine
  2. 2
    AutreThe organic layer is separated
  3. 3
    Séchagedried (magnesium sulfate)
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationconcentrated

Mode opératoire

A mixture of 36.61 g (295 mmol) of 4-fluorobenzaldehyde, 25 g (297.2 mmol) of ethyl vinyl ketone, 29 mL (206.9 mmol) of triethylamine and 11.94 g (44.25 mmol) of 3-benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chloride is stirred and heated at 70° C. for six hours. The cooled solution is diluted with 2 liters of diethylether and washed with 2×300 mL of water, 2×100 mL of 2M hydrochloric acid, 100 mL of water, 200 mL of a saturated solution of sodium bicarbonate and brine. The organic layer is separated, dried (magnesium sulfate), filtered, and concentrated to provide 55 g of 1-(4-fluorophenyl)-1,4-hexanedione after recrystallization from methanol; mp 56°-57° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05245047uspto-grants-1993_09