Réaction #2358529

ord-34fb5f3f64cc438d9c6d2d79c79d398b

Équation de réaction

O
water
CC(=O)CCl
1-Chloroacetone
CS(=O)(=O)c1cc(O)cc(F)c1
3-fluoro-5-methylsulfonyl-phenol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(=O)COc1cc(F)cc(S(C)(=O)=O)c1
1-(3-fluoro-5-methylsulfonyl-phenoxy)propan-2-one

Conditions de réaction

Température
120°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureto cool to ambient temperature
  2. 2
    ExtractionThe aqueous phase was extracted with ethyl acetate (3×100 ml)
  3. 3
    Lavagethe combined organic phase was washed with LiCl (5% aqueous solution, 4×50 ml), brine (50 ml)
  4. 4
    Séchagedried with Na2SO4
  5. 5
    Autreevaporated
  6. 6
    AutrePurification on flash chromatography (isooctane:ethyl acetate 1:0 to 3:2)

Mode opératoire

1-Chloroacetone (95%, 2.66 g, 27.34 mmol) was added to a stirred solution of 3-fluoro-5-methylsulfonyl-phenol (80%, 1.3 g, 5.46 mmol) and potassium carbonate (2.26 g, 16.40 mmol) in dry dimethyl formamide (10 ml), the mixture was heated to 120° C. for 20 minutes, the mixture was allowed to cool to ambient temperature and water (100 ml) was added. The aqueous phase was extracted with ethyl acetate (3×100 ml), the combined organic phase was washed with LiCl (5% aqueous solution, 4×50 ml), brine (50 ml) and dried with Na2SO4 and evaporated. Purification on flash chromatography (isooctane:ethyl acetate 1:0 to 3:2). 0.905 g, 67%. MS m/z (relative intensity, 70 eV) 246 (M+, 79), 204 (55), 203 (bp), 141 (30), 94 (67).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09120728B2uspto-grants-2015_09