Reacción #55289

ord-d1c2a84a75f940b4858cb02ecc076c17

Ecuación de reacción

O=C1OC(=O)c2ccccc21
phthalic anhydride
CN(C)c1cccc(N(C)C)c1
N,N,N',N'-tetramethyl-m-phenylenediamine
Clc1ccccc1
chlorobenzene
CN(C)c1ccc(C(=O)c2ccccc2C(=O)O)c(N(C)C)c1
2-(2,4-bis-(dimethylamino)benzoyl)benzoic acid
Cl.Cl.O.O.O
dihydrochloride trihydrate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas heated
  2. 2
    Temperaturaunder reflux for three hours
  3. 3
    OtroThe chlorobenzene was decanted
  4. 4
    Otrothe residue was air-dried
  5. 5
    workup.ADDITIONA solution of the residue in dilute hydrochloric acid (10%, 20 ml. plus 20 ml. of water) was diluted with more water (20 ml.)

Procedimiento

A mixture of phthalic anhydride (5.92 g.), N,N,N',N'-tetramethyl-m-phenylenediamine (6.56 g.), zinc chloride (5.40 g.) and chlorobenzene (70 ml.) was heated under reflux for three hours. The chlorobenzene was decanted and the residue was air-dried. A solution of the residue in dilute hydrochloric acid (10%, 20 ml. plus 20 ml. of water) was diluted with more water (20 ml.), affording 2-(2,4-bis-(dimethylamino)benzoyl)benzoic acid (II: Y'2 =Y'4 =(CH3)2N, Z4 =Z'5 =Z'6 =Z7 =H) dihydrochloride trihydrate (4 g., m.p. 136°-141° C.; after recrystallization from ethanol, m.p. 140°-141° C.). In another preparation the free base (m.p. 165°-168° C.) was obtained under less acidic conditions (pH 4-6).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04220357uspto-grants-1980_09