Réaction #54156
ord-b1299f3dbcbc49849b5ecf7df9c50d05
Équation de réaction
Réactifs
Conditions de réaction
Traitement
- 1workup.ADDITIONThere are charged to a half-liter reactor 9.4 g
- 2Températurethe mixture is cooled below 5° C
- 3workup.STIRRINGThe resulting mixture is stirred vigorously
- 4workup.ADDITIONthere is added a solution of 15.5 g
- 5workup.STIRRINGThe mixture is stirred at ambient temperature for 12 hours
- 6workup.ADDITIONthe mixture is poured in 100 g
- 7AutreThe organic fraction is removed by decantation
- 8Lavagethe aqueous fraction is washed twice with CCl4 (100 ml.)
- 9AutreThe organic fractions are collected
- 10Lavagewashed three times with water (to neutrality)
- 11AutreThe solvent is evaporated under reduced pressure
- 12SéchageThe organic solution is dried over anhydrous Na2SO4
- 13AutreThe solid obtained
- 14Autreis recrystallized in benzene
- 15AutreThere are obtained 16.9 g
Mode opératoire
There are charged to a half-liter reactor 9.4 g. (0.1 mole) of phenol in 150 ml. of nitrobenzene. The contents of the reactor are stirred and the mixture is cooled below 5° C. Then 27 g. (0.2 mole) of AlCl3 is added in small portions over 1/2 hour. The resulting mixture is stirred vigorously and then there is added a solution of 15.5 g. of C6H13COCl (~ 0.011 mole) in 50 ml. of nitrobenzene over an hour while the temperature is kept below 5° C. The mixture is stirred at ambient temperature for 12 hours and then the mixture is poured in 100 g. of ice and 50 ml. of concentrated HCl and stirred for 1/2 hour. The organic fraction is removed by decantation and the aqueous fraction is washed twice with CCl4 (100 ml.). The organic fractions are collected and washed three times with water (to neutrality). The solvent is evaporated under reduced pressure. The organic solution is dried over anhydrous Na2SO4. The solid obtained is recrystallized in benzene. There are obtained 16.9 g. of pure product (yield 82%), melting point: 93° C.