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Process for the preparation of 2,5-dialkyl (2,2,5,5-tetraalkyl) -3,4-fullerene 60 tetrahydrofuran

机译:制备2,5-二烷基(2,2,5,5-四烷基)-3,4-富勒烯的方法[60]四氢呋喃

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to organic chemistry, and more specifically to a method of producing new 2,5-dialkyl(2,2,5,5-tetraalkyl)-3,4-fullero[60]tetrahydrofuranes of general formula (1), , where R=Me, R'=H; R=Pr, R'-H; R=R'= Me. The method involves reacting fullerene C60 with dialkyl (diisoalkyl) esters of general formula (RR'CH)2O, where R=Me, R'=H; R=Pr, R'=H, R=R'=Me in the presence of titanocene dichloride catalyst in molar ratio C60:ester:Cp2TiCl2=0.01:(5 to 15):(0.0015 to 0.0025) in a toluene medium at temperature 140 to 160°C for 5 to 7 hours. Output of the desired product is 47 to 70%.;EFFECT: obtaining compounds which can be used as complexing agents, sorbents, biologically active compounds, as well as production of new materials with given electronic, magnetic and optical properties.;1 cl, 1 tbl,1 ex
机译:技术领域本发明涉及有机化学,更具体地涉及一种生产一般的新的2,5-二烷基(2,2,5,5-四烷基)-3,4-富勒[60]四氢呋喃的方法式(1),其中R = Me,R′= H; R = Pr,R'-H; R = R'=我。该方法涉及将富勒烯C 60 与通式(RR'CH) 2 O的二烷基(二异烷基)酯反应,其中R = Me,R'= H;在二茂钛二氯化物催化剂存在下,摩尔比为C 60 :酯:Cp 2 TiCl 时,R = Pr,R'= H,R = R'= Me将2 = 0.01:(5至15):( 0.0015至0.0025)在甲苯介质中于140至160°C的温度下放置5至7小时。所需产品的产量为47%至70%。效果:获得可用作络合剂,吸附剂,生物活性化合物的化合物,以及具有给定电子,磁性和光学性质的新材料的生产。1cl, 1 tbl,1 ex

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