Reaktion #73486

Reaktionsgleichung

3-cyano-3-(4-fluorophenyl)cyclobutan-1-ol

3-Cyano-3-(4-fluorophenyl)cyclobutan-1-ol

2,6-lutidine

tert-Butyldimethylsilyl trifluoromethanesulphonate

→

yellow oil

Ausbeute 104.0%

3-Cyano-3-(4-fluorophenyl)cyclobutan-1-yl t-butyldimethylsilyl ether

Ausbeute 104.0%

Lösungsmittel

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwas added dropwise
2. 2
   Sonstigethe stirred reaction mixture
3. 3
   WaschenThe reaction mixture was washed successively with water, hydrochloric acid (0.1M), saturated sodium bicarbonate solution and brine
4. 4
   Trocknenbefore being dried over sodium sulphate
5. 5
   FiltrationFiltration and evaporation

Vorschrift

3-cyano-3-(4-fluorophenyl)cyclobutan-1-ol (112, 19.8 g, 103.6 mmol) was dissolved in dichloromethane (200 mL) under argon, then 2,6-lutidine (27.78 g, 30.1 mL, 259 mmol) was added and the solution cooled to 0° C. tert-Butyldimethylsilyl trifluoromethanesulphonate (32.9 g, 28.6 mL, 124.3 mmol) was added dropwise and the stirred reaction mixture was then allowed to warm up to room temperature overnight. The reaction mixture was washed successively with water, hydrochloric acid (0.1M), saturated sodium bicarbonate solution and brine before being dried over sodium sulphate. Filtration and evaporation gave 32.9 g of a yellow oil which was used in the next step without further purification. Rt=1.30 min (Method 18). Detected mass: 306.3 (M+H+).

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