Catalytic hydroformamination of 2,5-dimethoxy-2,5-dihydrofurans

N-Substituted 3- and 4-formylpyrroles have been obtained by hydroformamination of 2,5-dimethoxy-2,5-dihydrofurans in the presence of HRh(CO)(PPh₃)₃.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1837–1840, August, 1990.     

Polymerization behaviour of 2,5-dimethylene- 2,5-dihydrofuran

Spontaneous homopolymerization of 2,5-dimethylene-2,5-dihydrofuran (DDF) was studied. The polymerization rates in two different initial monomer concentrations of DDF were analyzed with the first-order and second-order kinetics, and the homopolymerization of DDF was found to obey the first-order kinetics. The Arrhenius plot of the apparent rate constants at 30, 40, 50, and 60° gave an overall activation energy of 68.0 kJ/mol for the polymerization of DDF. From the comparison of the apparent rate constants at –78° and the time (the so-called half-life time) to decrease in half the monomer concentration for DDF with the corresponding values for p-xylylene (QM), DDF was found to be a less reactive monomer than QM. The copolymerizations of DDF with vinyl monomers such as acrylonitrile (AN), α-chloroacrylonitrile (CIAN), diethyl fumarate (DEF), and fumaronitrile (FN) were carried out in chloroform at 50° in the presence of AIBN to obtain the monomer reactivity ratios r₁(DDF) = 30.0 ± 3.0 and r₂ (AN) = 0 for the DDF-AN system, r₁ (DDF) = 1.55 ± 0.2 and r₂(CIAN) = 0 for the DDF-CIAN system, r₁(DDF) = 3.88 ± 0.2 and r₂(DEF) = 0 for the DDF-DEF system, and r₁(DDF) = 2.41 ± 0.1 and r₂ (FN) = 0 for the DDF-FN system, respectively. As the monomer reactivity ratios of r₂ for all systems were zero, Q and e values of DDF were calculated from the combination of two r₁ (DDF) values of any two copolymerization systems to be the 7.64 to 6.63 ×10²¹ range for Q and the –0.70 to –6.31 range for e, indicating that DDF is a highly conjugative and electron-donating monomer. © 1995 John Wiley & Sons, Inc.     

Synthesis and Chemistry of 2,5-Dimethylene-2,5-Dihydrofuran

2,5-Dimethylene-2,5-dihydrofuran (3), generated flash pyrolitically, underwent di- and trimerization reactions to give cyclic dimer and trimer. Compound 3 was trapped with methanol, ethanol, bromine, acetic acid, thiophenol and oxygen. Results from trapping experiments suggest that the diradical form of 3 is involved.     

On the thermal decomposition of 2,5-dihypochloro-2,5-dimethylhexane

The title compound was prepared, characterized, and on thermal decomposition at 100°C in the presence of a chlorine atom trap was found to give acetone, 1,2-dichloroethane, and 4-chloro-2-methyl-2-butanol.     

2,5-Dimethoxy-2,5-dihydrofurans in 1,3-dipolar cycloaddition reactions

Itis shown that 2,5-dimethoxy-2,5-dihydrofurans enter into 1,3-dipolar cycloaddition with benzonitrile N-oxides and with diphenylnitrilimines to form derivatives of 1,3-dimethoxy-6-phenyl-1,3,3a,6a-tetrahydrofuro[3,4-d]isoxazole and 1,3-dimethoxy-4,6-diphenyl-1,3,3a,-6a-tetrahydrofuro[3,4-d]pyrazole, respectively.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 150–151, February, 1971.     

Photochemical and chemical behaviour of 2,5-hydroperoxyhydroxy-2,5-dihydrofurans

From hydroxyhydroperoxides II and III a new bicyclic system, namely the 5,6-dioxabicyclo[2.1.1]hexane VII is obtained by photolysis or by protic acids. Epimer epoxides IV and XI are obtained on reaction with triethylamine.     

Acid-mediated cycloalkylation of C-aminoazoles with 2,5-dimethylhexane-2,5-diol

Alkylation of 5-aminotetrazole with 2,5-dimethylhexane-2,5-diol in perchloric acid was found to proceed on an endocyclic nitrogen atom as well as on the amino group, giving 5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-4H-tetrazolo[1,5-a][1,3]diazepine. Under analogous conditions, 3-amino-1,2,4-triazole undergoes cycloalkylation of the neighboring N1 and N2 atoms of the heterocycle resulting in 1-amino-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,2-a]pyridazinium perchlorate. The crystal structures of the products were determined by single crystal X-ray analysis.     

The Reaction of 2,5-Dimethoxy-2,5-Dihydrofuran with Dichloroketene

2,5-Dimethoxy-2,5-dihydrofuran (DDF) reacts with dichloroketene to give 7,9-dimethoxy-3,3,5,5-tetrachloro-8-oxabicyclo[4,3,0]-noan-2,4-dione (I), and methyl chloro-(2,5-dihydro-5-methoxy-2-furanylidene) acetate (II). The reactions of 2,5-dihydrofuran and 2,5-dimethoxy-tetrahydrofuran with dichloroketene were also-studied for comparison. Compound II was derived from the insertion of a molecule of dichloroketene into the C-O bond of DDF with subsequent dehydrochlorination. Compound I resulted from the cycloaddition of two molecules of dichloroketene to the C=C bond of DDF. A mechanism involving a 1,5-dipolar intermediate is proposed to account for this novel reaction.     

Protolytic cleavage of derivatives of 2,5-dimethoxy-2,5-dihydrofuran

By analysis of the products from the protolytic cleavage of methyl 3-(2,5-dialkoxy-2,5-dihydro-2-furyl)propionate (I) in the presence of mixed nucleophiles and investigation of their mutual transformations the main paths in the dissociation of the protonated molecule of (I), with the formation of both linear cleavage products (derivatives of 1,4-diketones and 4-ketopimelic acid) and furylcarbinol derivatives, were determined.Latvian Institute of Organic Synthesis. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 190–197, February, 1997.     

Syntheses and properties of donor-acceptor-type 2,5-diarylthiophene and 2,5-diarylthiazole

[structure: see text] Syntheses of differently substituted 2,5-diarylthiophenes and 2,5-diarylthiazoles are carried out with the palladium-catalyzed C-H substitution reaction using AgF as an activator. Remarkably strong photoluminescence is observed in 2,5-diarylthiophene. Differences between the physical properties of liquid crystalline characteristics and cyclic voltammograms of thiophene and thiazole are also studied.     

Introduction of ethynylene and thienylene spacers into 2,5-diarylthiazole and 2,5-diarylthiophene

Syntheses of 2,5-diarylthiazole and 2,5-diarylthiophene derivatives bearing ethynylene and thienylene spacers are performed. With the methods for coupling reactions of terminal alkynes and at the CH bond of heteroaromatic compounds, which we have developed, five kinds of thiazole and thiophene derivatives 3-7 are prepared. Spectroscopic characteristics of 3-7 are also measured.     

Synthesis and characteristics of the mass spectra of 2,5-dimercapto-2,5-dimethyltetrahydrothiophene

2,5-Dimercapto-2,5-dimethyltetrahyrothiophene was synthesized by the reaction of 1-iodopropan-2-one with hydrogen sulfide in an ether solution of hydrogen chloride at-70°C. Its structure was established by mass spectrometry, ¹H and ¹³C NMR spectroscopy. __________ Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, 216–219, February, 2007.     

New 2,5-diformylpyrrole bishydrazones

Russian Journal of General Chemistry -