Methyl phenyl carbonate (MPC) has been investigated as a carbomethoxylating agent of aromatic amines in the presence of group 3 metal (Sc or La) triflate catalysts. Under mild conditions (363 K), both Sc(OTf)3 and La(OTf)3 (OTf = O3SCF3) can promote the carbamation of aniline and a few industrially relevant aromatic diamines, such as 4,4-methylenedianiline (MDA) and 2,4-diaminotoluene (TDA), with MPC. Carbamate yield and selectivity are markedly affected by the experimental conditions (temperature, reaction medium, nature of the metal center). Sc(OTf)3 is a more effective and selective carbamation catalyst than La(OTf)3. Ad hoc experiments have shown that, in the presence of the M(OTf)3 (M = Sc, La) catalysts, MPC is not only more reactive but also a more selective carbomethoxylating agent than dimethyl carbonate (DMC).
“Carbomethoxylating reactivity of methyl phenyl carbonate towards aromatic amines in the presence of Group 3 metal (Sc, La) triflate catalysts”
QUARANTA, Eugenio
2004-01-01
Abstract
Methyl phenyl carbonate (MPC) has been investigated as a carbomethoxylating agent of aromatic amines in the presence of group 3 metal (Sc or La) triflate catalysts. Under mild conditions (363 K), both Sc(OTf)3 and La(OTf)3 (OTf = O3SCF3) can promote the carbamation of aniline and a few industrially relevant aromatic diamines, such as 4,4-methylenedianiline (MDA) and 2,4-diaminotoluene (TDA), with MPC. Carbamate yield and selectivity are markedly affected by the experimental conditions (temperature, reaction medium, nature of the metal center). Sc(OTf)3 is a more effective and selective carbamation catalyst than La(OTf)3. Ad hoc experiments have shown that, in the presence of the M(OTf)3 (M = Sc, La) catalysts, MPC is not only more reactive but also a more selective carbomethoxylating agent than dimethyl carbonate (DMC).I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
