首页> 外文会议>International Zeolite Conference pt.C; 20040425-30; Cape Town(ZA) >SYNTHESIS OF HETEROCYCLIC THREE-FUSED RING COMPOUNDS USING MOLECULAR SIEVE CATALYSTS
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SYNTHESIS OF HETEROCYCLIC THREE-FUSED RING COMPOUNDS USING MOLECULAR SIEVE CATALYSTS

机译:分子筛催化剂合成杂环三环化合物

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The reaction of cyclohexanone, formaldehyde and ammonia was carried out over zeolite/molecular sieve catalysts. The major products obtained were octahydrophenanthridine, octahydroacridine, eyclohexanoneoxime, cyclohexamine. The reaction of cyclohexanone, formaldehyde and ammonia was carried out over molecular sieve catalysts in an autoclave under 4-49 atm autogeneous pressure. The molar ratio of cyclohexanone:formaldehyde:NH_3 was 1:1:3 and 222 ml of methanol was used as a solvent. The selectivities for octahydrophenanthridine were 32.2, 44.4, 60.6 and 50.2 percent at 98.7, 97.7, 83.0 and 53.0 percent conversions of cyclohexanone at 215, 170, 150 and 100℃ respectively. The catalyst used was H-beta. The selectivities for octahydroacridine were 42.2, 39.4, 21.7 and 7.7 percent respectively. The effect of molar ratio, various solvents, various catalysts and reactants have been studied. The best catalysts observed were (Hβ)H-beta and HMCM-41. The cyclization reaction can also proceed over the active external surface of HZSM-5 and mordenite. With the increase of autoclavation temperature and pressure the yield of the cyclized products was increased. At high reaction temperature octahydroacridine increased and octahydrophenanthridine decreased. The reaction of cyclohexanone, formaldehyde and ammonia was also carried out using continuous-flow, fixed-bed reactor at 1 atm pressure. The vapour phase reaction was carried out at 400℃ reaction temperature with 0.5 h~(-1) weight hourly space velocity using H-MCM-41 catalyst. The selectivities for octahydroacridine were 36.3, 33.5 and 36.9 percent at 85.4, 94.0 and 86.3 percent conversions of cyclohexanone over LaMCM-41, Cu-MCM-41 and Cr-MCM-41 respectively. The various parameters like catalyst, variation of reactants, reaction temperature, etc. were studied. Under and similar to the supercritical conditions, there is substantial increase in the reactive collisions miscibility is increased, the mass transfer and heat transfer effect are enhanced, resulting into the increased yield and enhance the selectivity by using active and selective zeolite/molecular sieve catalysts. The varieties of heterocyclic compounds of acridine-type (three-fused ring system) or bis-annelated pyridines are obtained. The attempts are being made to synthesize useful compounds like tacrine (a drug for Alzheimer disease).
机译:环己酮,甲醛和氨的反应在沸石/分子筛催化剂上进行。获得的主要产物是八氢菲啶,八氢ac啶,环己酮肟,环己胺。环己酮,甲醛和氨的反应是在分子筛催化剂上于4-49 atm自生压力下于高压釜中进行的。环己酮:甲醛∶NH 3的摩尔比为1∶1∶3,使用222ml甲醇作为溶剂。在215、170、150和100℃,环己酮的转化率分别为98.7%,97.7%,83.0%和53.0%,八氢菲啶的选择性分别为32.2%,44.4%,60.6%和50.2%。使用的催化剂是H-β。八氢ac啶的选择性分别为42.2%,39.4%,21.7%和7.7%。已经研究了摩尔比,各种溶剂,各种催化剂和反应物的影响。观察到的最佳催化剂是(Hβ)H-beta和HMCM-41。环化反应也可以在HZSM-5和丝光沸石的活性外表面上进行。随着高压灭菌温度和压力的增加,环化产物的产率增加。在高反应温度下,八氢ac啶增加而八氢菲啶减少。环己酮,甲醛和氨的反应也使用连续流固定床反应器在1个大气压下进行。使用H-MCM-41催化剂,在400℃反应温度下以0.5 h〜(-1)重量时空速进行气相反应。八氢ac啶在LaMCM-41,Cu-MCM-41和Cr-MCM-41上的环己酮转化率分别为85.4%,94.0%和86.3%,选择性分别为36.3%,33.5%和36.9%。研究了催化剂,反应物变化,反应温度等各种参数。在超临界条件下并类似于超临界条件,通过使用活性和选择性的沸石/分子筛催化剂,反应性碰撞的混溶性显着增加,传质和传热效果得到增强,从而导致产率的提高和选择性的提高。获得了a啶型(三稠环系统)或双退火吡啶的杂环化合物。人们正在尝试合成有用的化合物,如他克林(他克林氏病的药物)。

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