Réaction #452447

ord-84b1ff093184403e8a43208e4adbd83f

Équation de réaction

O=C([O-])[O-].[K+].[K+]
Potassium carbonate
C=CC(C)(CCC=C(C)C)OC(=O)CC(C)=O
3,7-dimethyl-1,6-octadien-3-yl 3-oxo-butyrate
ClCc1ccccc1
benzyl chloride
C=CC(C)(CCC=C(C)C)OC(=O)C(Cc1ccccc1)C(C)=O
desired compound
C=CC(C)(CCC=C(C)C)OC(=O)C(Cc1ccccc1)C(C)=O
3,7-dimethyl-1,6-octadien-3-yl 3-oxo-2-benzylbutyrate

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrefitted with a magnetic stirrer, condenser and argon inlet
  2. 2
    TempératureThe mixture is heated
  3. 3
    Températureto reflux for 18 h
  4. 4
    FiltrationThe cooled mixture is filtered
  5. 5
    Concentrationconcentrated by rotary evaporation
  6. 6
    AutreThe resulting oil is purified on silica gel

Mode opératoire

Potassium carbonate (3.92 g, 0.028 mol), 3,7-dimethyl-1,6-octadien-3-yl 3-oxo-butyrate (4.80 g, 0.030 mol), benzyl chloride (4.80 g, 0.038 mol) and acetone (15 mL) are placed in a 50 mL round-bottomed flask fitted with a magnetic stirrer, condenser and argon inlet. The mixture is heated to reflux for 18 h. The cooled mixture is filtered and concentrated by rotary evaporation. The resulting oil is purified on silica gel to yield the desired compound. Structure is confirmed by thin layer chromatography and 1H and 13C NMR.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06126953uspto-grants-2000_10