Reaktion #1458426

ord-d9125d3c4a3b428e8432974472c5764b

Reaktionsgleichung

O
water
S=[PH](c1ccccc1)c1ccccc1
diphenylphosphine sulfide
O=C(CCl)c1ccccc1
chloroacetophenone
[K+].[OH-]
potassium hydroxide
O=C(CP(=S)(c1ccccc1)c1ccccc1)c1ccccc1
Phenylcarbonylmethyl-diphenylphosphine sulfide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas cooled to 8–10° C. in an ice-water bath
  2. 2
    Sonstigethe organic layer was separated
  3. 3
    Waschenwashed with more water (2 ml)
  4. 4
    Trocknendried over sodium sulfate
  5. 5
    SonstigeThe solvent was removed under reduced pressure
  6. 6
    Sonstigea rotary evaporator
  7. 7
    Sonstigethe oily residue was crystallized from ethyl acetate-hexane mixture
  8. 8
    Sonstigeto give 0.19 g (56.5%) of star

Vorschrift

A stirred mixture of diphenylphosphine sulfide (0.218 g, 0.001 mol) and chloroacetophenone (0.216 g, 0.0014 mol) in methylene chloride (4 ml) was cooled to 8–10° C. in an ice-water bath. Small pieces of solid potassium hydroxide (0.196 g, 0.0035 mol) were added while stirring under nitrogen atmosphere. After 45 minute, water (2 ml) was added and the organic layer was separated, washed with more water (2 ml) and dried over sodium sulfate. The solvent was removed under reduced pressure using a rotary evaporator and the oily residue was crystallized from ethyl acetate-hexane mixture to give 0.19 g (56.5%) of star shaped crystals. mp=83–84° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07157219B2uspto-grants-2007_01