Reaktion #64158

Reaktionsgleichung

4-(phenylsulfonyl)phenol

sodium hydride

trifluoroacetone

trimethylsulfoxonium iodide

sodium hydride

→

title compound

Ausbeute 9.5%

1,1,1-Trifluoro-2-methyl-3-(4-phenylsulfonylphenoxy)propan-2-ol

Ausbeute 9.5%

Lösungsmittel

dimethylsulfoxide

dimethylsulfoxide

water

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturto warm to room temperature where it
2. 2
   workup.STIRRINGThe mixture was stirred for 1 hour
3. 3
   Temperaturheated to 50° C. for 18 hours
4. 4
   Extraktionextracted with diethylether
5. 5
   SonstigeThe combined organic fractions were evaporated
6. 6
   Sonstigeto give an oil
7. 7
   WaschenChromatography, eluting with dichloromethane

Vorschrift

A suspension of trimethylsulfoxonium iodide (1.6 6 g, 7.56 mmol) and sodium hydride (0.36 g, 7.56 mmol of 50% in oil) was stirred in 25 mL of dimethylsulfoxide for 25 minutes. The mixture was cooled to 10° C. and was treated with a solution of trifluoroacetone (0.72 g, 6.41 mmol) in tetrahydrofuran (3 mL). After stirring for 20 minutes, the solution was allowed to warm to room temperature where it was treated with a solution of 4-(phenylsulfonyl)phenol (1.5 g, 6.40 mmol) and sodium hydride (0.31 g, 6.4 .mmol of 50% in oil) in dimethylsulfoxide (7.5 mL). The mixture was stirred for 1 hour and then heated to 50° C. for 18 hours. The reaction was poured into water, acidified to pH 6, and extracted with diethylether. The combined organic fractions were evaporated to give an oil. Chromatography, eluting with dichloromethane yielded the title compound as a tan solid (0.22 g); mp 94°-96° C.; NMR: 1.39 (s,3, CH3), 4.12 (q,2, CH2), 6.39 (s,1, OH), 7.17 (s,1, Ar), 7.20 (s,1, Ar), 7.63 (m,3, Ar), 7.91 (m,4, Ar); MS: m/z=361(M+1). Analysis for C16H15F3O4S: Calculated: C, 53.33; H, 4.20; Found: C, 53.54: H, 4.25.

Quelle