Acetylene derivatives of 1,2,4-oxadiazoles, i.e., 5-(2-arylethynyl)-3-aryl-1,2,4-oxadiazoles, have been obtained, for the first time reported, from 5-(2-arylethenyl)-3-aryl-1,2,4-oxadiazoles by their bromination at the carbon–carbon double bond followed by di-dehydrobromination with NaNH2 in liquid NH3. The reaction of the acetylenyl-1,2,4-oxadiazoles with arenes in neat triflic acid TfOH (CF3SO3H) at room temperature for 1 h resulted in the formation of E/Z-5-(2,2-diarylethenyl)-3-aryl-1,2,4-oxadiazoles as products of regioselective hydroarylation of the acetylene bond. The addition of TfOH to the acetylene bond of these oxadiazoles quantitatively resulted in E/Z-vinyl triflates. The reactions of the cationic intermediates have been studied by DFT calculations and the reaction mechanisms are discussed.
Siberian larch (Larix sibirica L.) is the main commercial species in Russia. Currently, larch woody greens are underutilized. They are considered a waste product from logging. This is due to the lack of knowledge on the composition of compounds and the variability of the raw material source itself as a result of the fall of the needles. The research purpose is to study the composition of hydrocarbons and esters from Siberian larch needles in summer and autumn collection from the Tomsk region. The shredded needles were extracted with propan-2-ol; then, after distillation of the solvent, substances soluble in petroleum ether (PE, 40–70 °С) were isolated. The latter were divided into free acids (31.5 % for green needles and 28.0 % for yellow needles) and neutral substances (59.8 and 48.1 %, respectively). Then, eutral substances were chromatographed on silica gel: hydrocarbons (2.43 and 3.02 %, hereinafter from neutral substances of green and yellow needles, respectively), esters (31.30 and 33.80 %) and triglycerides (11.70 % and 6.44 %). The ester and triglyceride fractions were exposed to alkaline hydrolysis and the acidic components of esters (9.12 and 24.80 %) and triacylglycerols (17.43 and 26.15 %) were produced. Fractions of unsaponifiable compounds, in addition to alcohols, contained unsaponifiables with unchanged Rf values on thin-layer chromatography (TLC). Fractions of unsaponifiables were chromatographed on silica gel, and then the isolated fractions were additionally chromatographed on silica gel with silver nitrate. The isolated compounds were identified by nuclear magnetic resonance (NMR) spectroscopy. In the acidic component of esters, the main components are linoleic and linolenic acids. Hydrocarbons are represented by sesquiterpenes in both collections of needles. A new aromatic hydrocarbon for coniferous plants, geranyl-p-cymene, has been identified. For the first time, polyprenols were isolated from Siberian larch greens, the structure of which differs from spruce and pine polyprenols by chain length according to NMR spectroscopy and mass spectrometry data. They contain from 14 to 20 isoprene links in the chain of molecules with predominance of prenol-17. The yield of polyprenols was 12.8–14.9 % of neutral substances of yellow and green needles, respectively. Tetracyclic triterpene alcohols and sterols were isolated from green needles. Triterpene alcohols were not found in yellow needles. For citation: Mikson D.S., Roshchin V.I. Hydrocarbons and Ethers of Extractive Substances of Siberian Larch Needles. Lesnoy Zhurnal [Russian Forestry Journal], 2021, no. 3, pp. 170–185. DOI: 10.37482/0536-1036-2021-3-170-185
The composition of triterpene alcohols and sterols in the fraction of Siberian larch (Larix sibirica Ldb.) conifer needles is considered in paper. The needles areextracted with propan-2-ol; resinous substances are extracted with petroleum ether (40–70°C);substances extracted with petroleum ether are divided into free acids and neutral substances. Neutral substances are separated in a silica gel column; eluent - petroleum ether supplemented with diethyl ether. The isolated esters fraction is hydrolyzed with potassium hydroxide in ethanol, and the “bound” acids are separated from unsaponifiable substances. Non-saponified substances are separated by chromatography into 5 fractions of phytosterols, the alcohol components of esters. The fractions are acetylated; the alcohol acetates are separatedonsilica gel with added silver nitrate. The isolated compounds was identified by NMR and GC-MS methods. Cycloartenol (6.82%, hereafter based onunsaponifiable substances), 24-methylenecycloartanol (6.75%), citrastadienol (7.69%), sitosterol (7.18%), cycloevcalenol (0.09%) are identified, obtussifoliol (0.01%), 24-methylenelophenol (0.10%), methyllophenol (1.84%) and campesterol (0.33%).
Acetylene derivatives of 1,2,4-oxadiazoles, 5-(2-arylethynyl)-3-aryl-1,2,4-oxadiazoles, have been obtained, for the first time, from 5-(2-arylethenyl)-3-aryl-1,2,4-oxadiazoles by their bromination at the carbon-carbon double bond followed by di-dehydrobromination with NaNH2 in liquid NH3. Reaction of the acetylene 1,2,4-oxadiazoles with arenes in neat triflic acid TfOH (CF3SO3H) at room temperature for 1 h result in the formation of E-/Z-5-(2,2-diarylethenyl)-3-aryl-1,2,4-oxadiazoles as products of regioselective hydroarylation of the acetylene bond. Addition of TfOH to acetylene bond of these oxadiazoles gives rise quantitatively to E-/Z-vinyl triflates. Reaction cationic intermediates have been studied by DFT calculations. The reaction mechanisms have been discussed.
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