Reacción #2460312

Ecuación de reacción

NaOH

3-bromobenzenethiol

sodium methoxide

methyl iodide

→

3-bromothioanisole

Disolventes

methanol

methanol

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGThe reaction mixture was stirred overnight at room temperature
2. 2
   Extracciónextracted three times with ether (60 ml×3)
3. 3
   LavadoThe combined organic layer was washed with saturated sodium chloride solution
4. 4
   Secadodried over anhydrous magnesium sulfate
5. 5
   OtroAfter removal of solvent
6. 6
   workup.DISTILLATIONthe product was purified by distillation at 80° C. (0.3 mmHg)
7. 7
   Otroisolated in 86.1% (4.62 g)
8. 8
   Otroyield

Procedimiento

3-bromobenzenethiol (5 g, 26.44 mmol) was added to a solution of sodium methoxide (1.43 g, 26.48 mmol) in 20 ml of anhydrous methanol. The mixture was stirred for 30 min under nitrogen at room temperature and a solution of methyl iodide (4.51 g, 31.77 mmol) in 20 ml anhydrous methanol was then added. The reaction mixture was stirred overnight at room temperature, poured into 2 M aqueous NaOH solution (30 ml) and extracted three times with ether (60 ml×3). The combined organic layer was washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After removal of solvent, the product was purified by distillation at 80° C. (0.3 mmHg) and isolated in 86.1% (4.62 g) yield. 1H NMR(CDCl3, 500 MHz) δ ppm: 2.44 (s, 3H, CH3), 7.1-7.4(m, 4H, Ar—H)GC-MS(relative intensity %): 202, 204(1:1, 100, M+), 187, 189(1:1, 11, 3-BrPhS+).

Fuente