Reacción #576683
ord-c1f03bc85f5641c488146610f299188a
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Temperaturathe mixture was refluxed for 3 hours
- 2Otrothe solid was separated off via a Büchner funnel
- 3ExtracciónThe aqueous phase was extracted three times with 150 ml each time of dichloromethane
- 4Extracciónthe solid was extracted a number of times with dichloromethane
- 5workup.ADDITIONwhile being treated with ultrasound
- 6SecadoThe combined organic phases were dried over magnesium sulfate
- 7Otrofreed of the solvent on a rotary evaporator
- 8Temperatura65 ml of 12M hydrochloric acid and the mixture was refluxed for three hours
- 9OtroThe solvent was subsequently removed under reduced pressure
- 10Lavadothe solution was washed with saturated sodium hydrogen carbonate solution
- 11Secadodried over magnesium sulfate
- 12OtroRemoval of the solvent
Procedimiento
25 g (91 mmol) of 1,8-dichloroanthraquinone and 65 g (1 mol) of Zn dust were suspended in 1 l of a 20% strength by weight aqueous ammonia solution and the mixture was refluxed for 3 hours. After cooling to room temperature, the solid was separated off via a Büchner funnel. The aqueous phase was extracted three times with 150 ml each time of dichloromethane; the solid was extracted a number of times with dichloromethane while being treated with ultrasound. The combined organic phases were dried over magnesium sulfate and freed of the solvent on a rotary evaporator. The solid, whitish yellow residue was suspended in 600 ml of propanol and 65 ml of 12M hydrochloric acid and the mixture was refluxed for three hours. The solvent was subsequently removed under reduced pressure, the residue was taken up in dichloromethane, the solution was washed with saturated sodium hydrogen carbonate solution and dried over magnesium sulfate. Removal of the solvent gave 1,8-dichloroanthracene as a yellow solid which was recrystallized from propanol.