Reacción #1973940

Ecuación de reacción

NaHCO3

ethyl acetate

3-methoxy-3-methylbutane-1-ol

pentafluorobenzenesulfonyl chloride

→

desired product

Rendimiento 163.0%

3-Methoxy-3-methylbutyl 2,3,4,5,6-pentafluorobenzenesulfonate

Rendimiento 163.0%

Disolventes

—

hexanes

CH2Cl2

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGthe mixture was stirred at rt for 30 min
2. 2
   ExtracciónThe organics were extracted with CH2Cl2 (75 mL)
3. 3
   Lavadowashed with 1 M HCl (2×25 mL), saturated aqueous NaHCO3 (1×25 mL) and saturated aqueous NaCl (1×25 mL)
4. 4
   SecadoThe organics were dried over Na2SO4
5. 5
   Concentraciónconcentrated
6. 6
   Otroto give a crude mixture

Procedimiento

To a solution of 3-methoxy-3-methylbutane-1-ol (1.07 g, 9 mmol) and TEA (0.61 g, 6 mmol) in CH2Cl2 (12 mL) was added pentafluorobenzenesulfonyl chloride (0.99 g, 3.7 mmol). The solution was stirred at rt for 2 h. Saturated aqueous NaHCO3 (12 mL) was added to the solution and the mixture was stirred at rt for 30 min. The organics were extracted with CH2Cl2 (75 mL) and washed with 1 M HCl (2×25 mL), saturated aqueous NaHCO3 (1×25 mL) and saturated aqueous NaCl (1×25 mL). The organics were dried over Na2SO4 and concentrated to give a crude mixture. Silica gel chromatography with ethyl acetate in hexanes yielded the desired product (2.1 g, 81%). 1H NMR (400 MHz CDCl3) δ 4.42 (t, 2H, J=7.3 Hz), 3.13 (s, 3H), 1.97 (t, 2H, J=7.4 Hz), 1.17 (s, 6H); 19F NMR (400 MHz CDCl3) δ −137.9 (m, 2H), −146.65 (m, 1H), −161.01 (m, 2H). Anal. Calcd. For C12H13F5O4S: C, 41.38; H, 3.76. Found: C, 41.37; H, 3.77.

Fuente