Réaction #1458426

ord-d9125d3c4a3b428e8432974472c5764b

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas cooled to 8–10° C. in an ice-water bath
  2. 2
    Autrethe organic layer was separated
  3. 3
    Lavagewashed with more water (2 ml)
  4. 4
    Séchagedried over sodium sulfate
  5. 5
    AutreThe solvent was removed under reduced pressure
  6. 6
    Autrea rotary evaporator
  7. 7
    Autrethe oily residue was crystallized from ethyl acetate-hexane mixture
  8. 8
    Autreto give 0.19 g (56.5%) of star

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07157219B2uspto-grants-2007_01