Yoshio Urawa

A convenient method for preparing aromatic ketones from acyl chlorides and arylboronic acids via Suzuki–Miyaura type coupling reaction

Abstract Aromatic ketones are synthesized efficiently via palladium-catalyzed cross-coupling reaction of boronic acids with acyl chlorides in the presence of K 3 PO 4 hydrate in toluene. This allows the use of aliphatic acyl chlorides as the starting material. Hydrated water plays a significant role as an H 2 O source to activate the catalytic system.

Investigations into the Suzuki–Miyaura coupling aiming at multikilogram synthesis of E2040 using (o-cyanophenyl)boronic esters

Abstract The Suzuki–Miyaura cross-coupling reaction between 1-{3-bromo-4-chloro-5-[1-( R )-fluoropropyl]}phenylpiperazine (( R )- 1b ) and thermally unstable ( o -cyanophenyl)boronic ester 6b in the presence of dichlorobis(triphenylphosphine)palladium and potassium phosphate hydrate in boiling toluene was found to afford 1-{3-(2-cyanophenyl)-4-chloro-5-[1-( R )-fluoropropyl]}phenylpiperazine (( R )- 5 ), an intermediate for the synthesis of E2040, in excellent yields. The reaction conditions for the cross-coupling were optimized by the design of experiments (DOE) approach and found to be applicable to electron-rich and/or sterically hindered aryl bromides. Safety evaluation for the production of ( R )- 5 is also described.