Reaktion #3005

ord-9faac40bc60f4f9481fb3e21ace77f7b

Reaktionsgleichung

O=C([O-])[O-].[K+].[K+]
potassium carbonate
ClCc1ccccc1
benzyl chloride
Cc1cc(O)cc(=O)o1
4-hydroxy-6-methyl-2H-pyran-2-one
C1COCCOCCOCCOCCOCCO1
18-crown-6
Cc1cc(OCc2ccccc2)cc(=O)o1
4-Benzyloxy-6-methyl-2H-pyran-2-one

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationfiltered
  2. 2
    Waschenthe residue was washed well with ethyl acetate
  3. 3
    SonstigeThe combined filtrates were extensively evaporated in a vacuum
  4. 4
    workup.ADDITIONsubsequently poured onto ice water
  5. 5
    SonstigeThe aspirated precipitate was recrystallized from t-butylmethyl ether
  6. 6
    Sonstigeafter drying

Vorschrift

124.4 g (0.900 mol) potassium carbonate and 63 ml (0.547 mol) benzyl chloride were added in succession to a solution of 56.7 g (0.450 mol) 4-hydroxy-6-methyl-2H-pyran-2-one and 1.0 g (0.004 mol) 18-crown-6 in 900 ml anhydrous dimethyl-formamide. It was stirred vigorously for 4.5 hours at an internal temperature of 70°-75° C. It was suction filtered and the residue was washed well with ethyl acetate. The combined filtrates were extensively evaporated in a vacuum and subsequently poured onto ice water. The aspirated precipitate was recrystallized from t-butylmethyl ether after drying. 69.0 g (71%) V, melting point 92°-93° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731344uspto-grants-1998_03