Reacción #83906
ord-6cb87811cba8461b8d090235ec7639ac
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Lavadowashed twice with 10% sodium hydroxide (200 ml), water, and brine
- 2Secadodried (Na2SO4)
- 3ConcentraciónThe product was concentrated to an oil
- 4workup.STIRRINGA portion was stirred with ether (100 ml)
- 5Otroa crystalline product was formed
- 6FiltraciónThe crystalline product was recovered by filtration
- 7Otropurified by recrystallization
Procedimiento
To the compound p-bromoacetophenone (36.85 g, 185 mmol) in trichloromethane (300 ml) was added 1,3-propanedithiol (25 g, 230 mmol) and boron trifluoride etherate (3 ml). The resulting mixture was stirred at room temperature for 48 hours. The mixture was diluted with dichloromethane (500 ml), washed twice with 10% sodium hydroxide (200 ml), water, and brine, and then dried (Na2SO4). The product was concentrated to an oil. A portion was stirred with ether (100 ml) and a crystalline product was formed. The crystalline product was recovered by filtration and purified by recrystallization to yield 4-bromo-1-(1,3-dithian-2-yl)ethylbenzene.