Deuterium exchange of 4-pyrimidones and 4-pyrimidthiones

The hydrogen-deuterium exchange of H-2 in 4-pyrimidone, a number of 1- and 3-alkyl-4-pyrimidones and several of their thione analogs in deuterium oxide at moderate temperatures is reported. This reaction is apparently not susceptible to acid or base catalysis. Cations of the 4-pyrimidones were found not to exchange H-2 at all in acid media. Catalytic amounts of bases do not alter the exchange rates whereas more concentrated alkali decompose the pyrimidone. However, 1,4(3,4)-dihydro-1,3-dimethyl-4-oxopyrimidinium iodide (and its 6-methyl analog) exchange H-2 quite rapidly in neutral deuterium oxide, almost instantly when triethylamine is added as a catalyst, and very slowly in dilute solutions of deuterium chloride in deuterium oxide. Mechanisms are proposed to account for these phenomena.     

Catalytic desulfurization of condensed thiophenes by means of methanol

Desulfurization of dibenzothiophene, two methyldibenzothiophenes, and phenanthro[4,5-bcd]-thiophene to give 60-80% yields of hydrocarbon products was effected by means of a sulfided molydena catalyst plus methanol at 450° and a pressure of ca. one atmosphere. The methanol functions both as an in situ hydrogen donor and as a methylating agent.     

Thermal desorption of alcohols and ethers from the surface of aluminum oxide

Conclusions A Chromatographic investigation was made of the thermal desorption of methanol and isopropanol and of diisopropyl ether from the surface of A1₂O₃.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 200–201, January, 1987.     

Buchbesprechungen

Ohne Zusammenfassung     

1-Hydro-3-vinylhexamethylcyclotetrasiloxane and its polymerization

1,3-Dimethyl-3-vinyl-1,3-dichlorosiloxane is prepared by partial cohydrolysis of methylvinyldichlorosilane and methyldichlorosilane, and its cohydrolysis with sym-tetra-methyldichlorodisiloxane gives 1-hydro-3-vinylhexamethyl-cyclotetrasiloxane. A study is made of the kinetics of the polymerization of the latter in CCL₄ in the presence of H₂PtCl₆ · 6H₂O