Reacción #1687650

Ecuación de reacción

morpholine

piperidine

hydrogen chloride

2,5-dichlorobenzoylchloride

anisole

diphenyl ether

→

2,5-dichlorobenzoylpiperidine

2,5-dichlorobenzoylmorpholine

Disolventes

toluene

pyridine

toluene

benzene

toluene

Condiciones de reacción

Tratamiento posterior

1. 1
   Otroat 0-5° C.
2. 2
   OtroThe solid products obtained
3. 3
   Otroupon quenching with water
4. 4
   Otroare purified by recrystallization from toluene/hexanes
5. 5
   LavadoAfter washing away the pyridinium salt
6. 6
   Otroany excess amine, the product is crystallized from the toluene solution

Procedimiento

A wide variety of 2,5-dichlorobenzoyl-containing compounds (e.g. 2,5-dichlorobenzophenones and 2,5-dichlorobenzamides) can be readily prepared from 2,5-dichlorobenzoylchloride. Pure 2,5-dichlorobenzoylchloride is obtained by vacuum distillation of the mixture obtained from the reaction of commercially available 2,5-dichlorobenzoic acid with a slight excess of thionyl chloride in refluxing toluene. 2,5-dichlorobenzophenones (e.g. 2,5-dichlorobenzophenone, 2,5-dichloro-4'-methylbenzophenone, 2,5-dichloro-4'-methoxybenzophenone, and 2,5-dichloro-4'-phenoxybenzophenone) are prepared by the Friedel-Crafts benzoylations of an excess of benzene or substituted benzenes (e.g. toluene, anisole, or diphenyl ether, respectively) with 2,5-dichlorobenzoylchloride at 0-5° C. using 2-3 mole equivalents of aluminum chloride as a catalyst. The solid products obtained upon quenching with water are purified by recrystallization from toluene/hexanes. 2,5-dichlorobenzoylmorpholine and 2,5-dichlorobenzoylpiperidine are prepared from the reaction of 2,5-dichloro-benzoylchloride and either morpholine or piperidine, respectively, in toluene with pyridine added to trap the hydrogen chloride that is evolved. After washing away the pyridinium salt and any excess amine, the product is crystallized from the toluene solution.

Fuente