Reacción #54156

Ecuación de reacción

C6H13COCl

HCl

phenol

nitrobenzene

nitrobenzene

AlCl3

→

product

Rendimiento 82.0%

4-heptanoylphenol

Rendimiento 82.0%

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONThere are charged to a half-liter reactor 9.4 g
2. 2
   Temperaturathe mixture is cooled below 5° C
3. 3
   workup.STIRRINGThe resulting mixture is stirred vigorously
4. 4
   workup.ADDITIONthere is added a solution of 15.5 g
5. 5
   workup.STIRRINGThe mixture is stirred at ambient temperature for 12 hours
6. 6
   workup.ADDITIONthe mixture is poured in 100 g
7. 7
   OtroThe organic fraction is removed by decantation
8. 8
   Lavadothe aqueous fraction is washed twice with CCl4 (100 ml.)
9. 9
   OtroThe organic fractions are collected
10. 10
    Lavadowashed three times with water (to neutrality)
11. 11
    OtroThe solvent is evaporated under reduced pressure
12. 12
    SecadoThe organic solution is dried over anhydrous Na2SO4
13. 13
    OtroThe solid obtained
14. 14
    Otrois recrystallized in benzene
15. 15
    OtroThere are obtained 16.9 g

Procedimiento

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.

Fuente