Reaktion #4989

ord-3e5a74dd499d489bad82923a415203e2

Reaktionsgleichung

C=CC(Cl)c1ccccc1
vinylbenzyl chloride
CC(=O)/C=C(/C)[O-].[Na+]
sodium acetylacetonate
[I-].[Na+]
sodium iodide
C=CC(Cl)c1ccccc1
vinylbenzyl chloride
CC(C)=O
acetone
CC(C)=O
acetone
C=Cc1cccc(CC(C(C)=O)C(C)=O)c1
3-vinylbenzyl Acetylacetone

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAn ice bath was used
  2. 2
    Sonstigethe pot temperature below 50°
  3. 3
    workup.ADDITIONduring the addition
  4. 4
    TemperaturThe solution was maintained at 45°-50° C. until NMR samples
  5. 5
    Sonstigeplaced in the refrigerator overnight
  6. 6
    FiltrationThe sodium chloride was then filtered
  7. 7
    Sonstigethe acetone removed at room temperature under reduced pressure
  8. 8
    workup.ADDITIONThe crude product was then added to an excess of toluene (800 ml)
  9. 9
    Sonstigeto precipitate any remaining sodium salts
  10. 10
    FiltrationThe solution was again filtered
  11. 11
    Sonstigethe toluene was removed at temperatures below 50° C. under reduced pressure

Vorschrift

To 308 g of sodium acetylacetonate and 30 g of sodium iodide in 100 mL acetone (dried over 3A molecular sieves) was added dropwise 282 ml vinylbenzyl chloride (70% Meta, 30% Para), in 600 ml acetone. An ice bath was used to keep the pot temperature below 50° during the addition. The solution was maintained at 45°-50° C. until NMR samples showed no residual vinylbenzyl chloride (about 1 hour). The pot was then cooled to room temperature and placed in the refrigerator overnight. The sodium chloride was then filtered and the acetone removed at room temperature under reduced pressure. The crude product was then added to an excess of toluene (800 ml) to precipitate any remaining sodium salts. The solution was again filtered and the toluene was removed at temperatures below 50° C. under reduced pressure.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05242877uspto-grants-1993_09