I, n=7, II, which involves reacting hydrogen sulphide-saturated aqueous formaldehyde solution (37%) with freshly prepared solution of thiocarbamide - n-BuONa in ratio thiocarbamide: CH2O:H2S:n-BuONa of 1:3:2:2 at 40°C and constant stirring for 6 hours, followed by reacting the obtained macroheterocycle (I) with CH3I (1:10) for 7 days.;EFFECT: method of producing novel compounds which can be used as selective sorbents and extractants of ore and precious metals and as biocides.;1 cl, 1 ex"/> METHOD FOR PHASE PRODUCTION OF 1,7,13,19,25,31,37,43-OCTATHIA-3,5,9,11,15,17,21,23,27,29,33,35,39,41,45,47-HEXADECAAZACYCLOOCTATETRACONTANE-4,10,16,22,28,34,40,46-OCTATHIONE AND 5,6-DIHYDRO-2H-THIADIAZINE HYDROIODIDE
首页> 外国专利> METHOD FOR PHASE PRODUCTION OF 1,7,13,19,25,31,37,43-OCTATHIA-3,5,9,11,15,17,21,23,27,29,33,35,39,41,45,47-HEXADECAAZACYCLOOCTATETRACONTANE-4,10,16,22,28,34,40,46-OCTATHIONE AND 5,6-DIHYDRO-2H-THIADIAZINE HYDROIODIDE

METHOD FOR PHASE PRODUCTION OF 1,7,13,19,25,31,37,43-OCTATHIA-3,5,9,11,15,17,21,23,27,29,33,35,39,41,45,47-HEXADECAAZACYCLOOCTATETRACONTANE-4,10,16,22,28,34,40,46-OCTATHIONE AND 5,6-DIHYDRO-2H-THIADIAZINE HYDROIODIDE

机译:1,7,13,19,25,31,37,43-OCTATHIA-3,5,9,11,15,17,21,23,27,29,33,35,39,41的相生产方法,45,47-正十六碳六环己酸酯-4,10,16,22,28,34,40,46-六氢噻吩和5,6-二氢-2H-噻二嗪氢溴酸盐

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to organic synthesis and specifically to a method of for phase production of 1,7,13,19,25,31,37,43-octathia-3,5,9,11,15,17,21,23,27,29,33,35,39,41,45,47-hexadecaazacyclooctatetracontane-4,10,16,22,28,34,40,46-octathione (I) and then 5,6-dihydro-2H-thiadiazine hydroiodide (II) of formulae: I, n=7, II, which involves reacting hydrogen sulphide-saturated aqueous formaldehyde solution (37%) with freshly prepared solution of thiocarbamide - n-BuONa in ratio thiocarbamide: CH2O:H2S:n-BuONa of 1:3:2:2 at 40°C and constant stirring for 6 hours, followed by reacting the obtained macroheterocycle (I) with CH3I (1:10) for 7 days.;EFFECT: method of producing novel compounds which can be used as selective sorbents and extractants of ore and precious metals and as biocides.;1 cl, 1 ex
机译:技术领域本发明涉及有机合成,特别是涉及一种用于生产1,7,13,19,25,31,37,43-octathia-3,5,9,11,15, 17,21,23,27,29,33,35,39,41,45,47-hexadecaazacyclooctatetracontane-4,10,16,22,28,34,40,46-octathione(I)然后5,6-二氢-2H-噻二嗪氢碘化物(II),其公式为:<图像文件=“ 00000015.GIF” he =“ 43” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 44” /> I,n = 7,<图像文件=“ 00000016.GIF” he =“ 39” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 37” /> II,该过程涉及使硫化氢饱和的甲醛水溶液(37%)与新鲜制备的溶液反应硫脲:CH 2 O:H 2 S:n-BuONa的比例在40°C并持续搅拌下的硫脲-n-BuONa的合成反应6小时,然后使所得的大杂环(I)与CH 3 I(1:10)反应7天。效果:制备可用作选择性吸附剂和萃取剂的新型化合物的方法矿石和贵金属s和作为杀菌剂。; 1 cl,1 ex

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