A novel synthesis of dialkyl carbonates from carbon dioxide, alcohols, and tert-amines mediated by acetylene
A novel acetylene-mediated reaction of carbon dioxide with alcohols and tert-amines leads to effective formations of dialkyl carbonates and alkyl N,N-dialkylcarbamates without catalyst.
Sasaki, Yoshiyuki
p. 825 - 826
(2007/10/03)
Alkoxycarbonylation of alcohols and phenols by nitrosoformates
Unstable neutral radicals [ROCONHO?] 2 and nitrosoformates 3 are formed by oxidation of N-hydroxycarbamates with lead dioxide. In the presence of alcohols or phenols and water they solvolyzed to mixtures of symmetrical 4 and asymmetrical 5 carbonates. The content of asymmetrical carbonates 5 increases with increasing reactivity of the nitrosoformates 3 formed, temperature, the content of water in the reaction mixture, and with decreasing reactivity of alcohol. The reactivities of individual alcohols have been evaluated with the help of competitive alcoholysis. The new method of alcohol or phenol alkoxylation has been verified experimentally by preparing six asymmetrical carbonates which were obtained in 34 to 47% yields.
Mindl, Jaromir,Halama, Ales,Cernosek, Zdenek
p. 1053 - 1063
(2007/10/03)
More Articles about upstream products of 35363-40-7