Reacción #710538

Ecuación de reacción

methanesulfonyl chloride

4-bromobenzylalcohol

Et3N

→

methanesulfonic acid 4-bromo-benzyl ester

Rendimiento 94.0%

Disolventes

DCM

Condiciones de reacción

Tratamiento posterior

1. 1
   Otroquenched with water
2. 2
   workup.ADDITIONSaturated aqueous NaHCO3 was added
3. 3
   Extracciónthe product was extracted with DCM
4. 4
   Filtraciónthe combined organic extracts were filtered through a phase separator cartridge
5. 5
   Concentraciónconcentrated

Procedimiento

To a solution of 4-bromobenzylalcohol (2 g, 10.7 mmol) in DCM (30 mL) at 0° C. was added Et3N (2.2 mL, 16.0 mmol) followed by methanesulfonyl chloride (910 μL, 11.8 mmol). The reaction was allowed to warm to room temperature, stirred for 2 hours and then quenched with water. Saturated aqueous NaHCO3 was added, the product was extracted with DCM, the combined organic extracts were filtered through a phase separator cartridge and concentrated to give methanesulfonic acid 4-bromo-benzyl ester (2.67 g, 10 mmol, 94%). A solution of the crude product (2.67 g, 10 mmol) in DMSO (40 mL) was stirred at room temperature for 16 hours with potassium thioacetate (1.26 g, 11 mmol). The reaction was treated with water and extracted with DCM, filtered through a phase separator, concentrated and purified by silica gel column chromatography (0-50% DCM in cyclohexane) to give thioacetic acid S-(4-bromo-benzyl) ester (1.81 g, 7.39 mmol, 69%). 1H NMR (300 MHz, CDCl3): δ 7.41 (d, 2 H), 7.16 (d, 2 H), 4.05 (s, 2 H), 2.35 (s, 3 H).

Fuente