Reacción #703592

ord-3136111fc16f4cebb7a7f3363b4d7f1b

Ecuación de reacción

Cl
hydrochloric acid
O=Cc1cc(Br)cc(Br)c1O
3,5-dibromo-salicylaldehyde
CC(C)(C)N
tert. butylamine
N
ammonia
CC(C)(C)NCc1cc(Br)cc(Br)c1O.Cl
N-tert.butyl-3,5-dibromo-2-hydroxy-benzylamine hydrochloride

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe precipitate formed
  2. 2
    Otroto crystallize the product out

Procedimiento

7 gm of 3,5-dibromo-salicylaldehyde, 17.5 gm of tert. butylamine and 7.7 gm of formic acid were heated for 6 hours at 70°-80° C. Subsequently, the reaction mixture was admixed with aqueous 2 N ammonia, vigorously shaken, and the precipitate formed thereby was sucked off. The residue was dissolved in ethanol, acidified with ethanolic hydrochloric acid and admixed with ether in order to crystallize the product out. N-tert.butyl-3,5-dibromo-2-hydroxy-benzylamine hydrochloride, m.p. 216°-220° C (decomp.), was obtained after recrystallization from absolute ethanol/ether.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04073942uspto-grants-1978_02