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SYNTHESIS METHOD OF LINOLEUM AND LINOLENIC ACIDS, MARKED BY CARBON COMPOUNDS 13C AND 14C

机译:以碳化合物13C和14C为标记的亚麻油和亚麻酸的合成方法

摘要

FIELD: chemistry.;SUBSTANCE: synthesis method by 13C-linoleic, 13C-linolenic, 14C-linoleic and 14C-linolenic acids includes the carbon dioxide condensation, marked by 14C or 13C, with the Grignard reagent, produced from 1-bromo-8.11-heptadecandiene (in case of linoleic acid) or from 1-bromo-8.11.14-heptadecanthriene (in the case of linolenic acid), carried out in the following sequence of steps: a - production of the Grignard reagent by the reaction of metallic magnesium with 1-bromo-8.11-heptadecandiene (in case of linoleic acid) or with 1-bromo-8.11.14-heptadecantriene (in case of linolenic acid) in the presence of metallic iodine; b - carboxylation of the Grignard reagent, produced at point a, for 5-15 min at temperature -20°C at constant stirring, carbon dioxide, marked by 14C or 13C, produced by the sulfuric acid of barium carbonate decomposition, marked by 14C and 13C, at the CO2 pressure of not more than 500 mm Hg. (maintaining by the drop metering of sulfuric acid); after stopping the pressure change in the system, the reaction flask is cooled with the liquid nitrogen in order to provide the quantitative transfer of the remaining in the system 14CO2 or 13CO2 in it, close the tap connecting the device to the CO2 source, and the reaction mixture is stirred for 15 minutes at the temperature -20°C with the purpose to fully incorporate the isotopically marked carbon dioxide into the product of the synthesis: linoleic or linolenic acid.;EFFECT: target products manufacture process acceleration, reduction of carbon dioxide losses, increase of its total chemical and radiation yield in comparison with the prototype, and elimination of the isotope-marked atoms distribution along the entire length of the acyl chain, the simplification and cheapening of the target products the linoleic and linolenic acids manufacture process, is ensured by the decrease in the duration, the increase of the radiation and chemical yield of the product along the source of the isotope in comparison with the prototype, the radioactive wastes release into the external environment is almost completely excluded, as its inclusion into the target product is approaching to the quantitative.;10 tbl, 2 ex, 4 dwg
机译:领域:化学。物质: 13 C-亚油酸, 13 C-油酸, 14 C-亚油酸和 14的合成方法 C-亚麻酸包括由1-bromo-8.11-十七碳二烯生产的格氏试剂引起的二氧化碳缩合,以 14 C或 13 C标记(亚油酸的情况下)或1-溴-8.11.14-十七碳六烯(亚油酸的情况下),按以下步骤顺序进行:a-通过金属镁与金属镁的反应制备格氏试剂在金属碘存在下,1-溴-8.11-十七碳二烯(亚油酸的情况)或1-溴8.1.14-十七碳三烯(亚油酸的情况); b-在恒定搅拌下于-20°C的温度下于a点产生的格氏试剂的羧化5-15分钟,二氧化碳以 14 C或 13 C,由碳酸钡分解的硫酸产生,以 14 C和 13 C标记,且CO 2 压力不大于超过500毫米汞柱。 (通过硫酸的滴定计量进行维护);停止系统中的压力变化后,将反应烧瓶用液氮冷却,以便定量输送系统 14 CO 2 或<其中的Sup> 13 CO 2 ,关闭将设备连接到CO 2 源的水龙头,将反应混合物在此温度下搅拌15分钟。 -20°C,目的是将同位素标记的二氧化碳完全掺入合成产物:亚油酸或亚麻酸;效果:目标产物可加速生产过程,减少二氧化碳损失,提高其总化学和辐射产率与原型相比,消除了沿着酰基链的整个长度的同位素标记的原子分布,通过减少持续时间,减少了对亚油酸和亚麻酸的生产过程,确保了目标产品的简化和廉价化。辐射和化学的增加与原型相比,沿着同位素源的产物的化学收率,几乎完全排除了向外部环境释放的放射性废物,因为将其纳入目标产物的程度已接近定量。10tbl,2 ex, 4 dwg

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