Rearrangements in cobaltic fluoride fluorinations of cycloalkanes with seven or more ring carbons

Cyclo-heptane, -octane, -decane, -dodecane and -octadecane have been fluorinated in the vapour phase with cobaltic fluoride. The perfluorocarbons obtained revealed varying degrees of skeletal rearrangements. Thus, cycloheptane gave perfluoro-cycloheptane and -methylcyclohexane; cyclooctane gave at least eight fluorocarbons including-bicyclo(3,3,0)octane and -cyclooctane; cyclodecane gave a complex mixture from which were isolated perfluoro cis- and trans-bicyclo(4,4,0)decanes but no perfluorocyclodecane; cyclododecane and cyclooctadecane gave complex fluorocarbon mixtures in which none of the fluorocarbons with the original cycloalkene skeleton could be detected.Tetradecafluorobicyclo(3,3,0)octane gave dodecafluorobicyclo (3,3,0)oct-1(5)-ene and decafluorobicyclo(3,3,0)octa-di-1(5), 2-ene when pyrolysed over iron gauze.The fluorination of cyclooctane also afforded 1$\text{H}$-pentadecafluorocyclooctane which was dehydrofluorinated to tetradecafluorocyclooctene. This was converted to a range of derivatives including dodecafluorosuberic acid, 1,2-dichlorotetradecafluorocyclooctane, 1-methoxy tridecafluorocyclooctene and tetradecafluorocyclooctanone.     

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     

Als Beitrag zur Analytik von Organozinn-Stabilisatoren

Ohne Zusammenfassung     

Tetracyclines Communication 33. Synthesis of 8-chloro-5-methoxy-3,10-dioxo-1,2,3,4,4a,9,9a,10-octahydroanthracene [5-chloro-1,3,4,4a,9a,10-hexahydro-8-methoxy-2,9-anthracenedione]

Summary 8-Chloro-5-methoxy-3,10-dioxo-1,2,3,4,4a,9,9a,10-octahydroanthracene (Ib) was synthesized; this can serve as an intermediary in the preparation of the tetracyclic analog (IIb) of aureomycin,Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 806–810, May, 1965 Original article submitted April 22, 1963For preceding communication see [1],The authors thank L. B. Senyavina for infrared spectrum measurements.