posted on 2018-11-26, 00:00authored bySzilvia Bunda, Antal Udvardy, Krisztina Voronova, Ferenc Joó
With
use of a Pd(II)-sulfosalan complex as a water-soluble catalyst,
we have developed an efficient synthesis of biaryls via Suzuki–Miyaura
cross-coupling in water under aerobic conditions. The water-insoluble
target molecules were isolated by simple filtration in analytical
purity after washing with 0.01 M aqueous HCl (20 examples). In most
cases, palladium contamination was below 5 ppm considered acceptable
for active pharmaceutical ingredients. The established method is scalable,
reproducible, and provides biaryl products in isolated yields up to
91%.