首页> 外文期刊>Journal of Fluorine Chemistry >Selective dehydrofluorination of 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) to 2-chloro-3,3,3-trifluoropropene (HFO-1233xf) using nanoscopic aluminium fluoride catalysts at mild conditions
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Selective dehydrofluorination of 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) to 2-chloro-3,3,3-trifluoropropene (HFO-1233xf) using nanoscopic aluminium fluoride catalysts at mild conditions

机译:在温和条件下使用纳米镜铝氟化物催化剂选择2-氯-1,1,2-四氟丙烷(HCFC-244bb)至2-氯-3,3,3-三氟丙烯(HFO-1233xF)的选择性脱氟化烃

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摘要

Aluminium chlorofluoride (ACF, AlClxF3-x, x = 0.05-0.3) and high-surface aluminium fluoride (HS-AlF3) were tested as heterogeneous catalysts for the reactivity towards 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb), which is a potent greenhouse gas. Selective activation and dehydrofluorination of the C-F bond was observed, under remarkable conditions, such as mild temperatures (70 degrees C) and without the need for a hydrogen source as a driving force. Consecutive reactions were developed by using C6D6 as a solvent or adding Et3SiH. Thus, the production of the dehydrofluorination product 2-chloro-3,3,3-trifluoropropene (HFO-1233xf) can be coupled to a hydroarylation or hydrodefluorination reaction in one-pot procedures.
机译:氯氟化铝(ACF,ALCLXF3-X,X = 0.05-0.3)和高表面氟化铝(HS-ALF3)作为异质催化剂,用于对2-氯-1,1,1,2-四氟丙烷的反应性(HCFC -244bb),这是一个有效的温室气体。 在显着条件下观察到C-F键的选择性活化和脱氟化氢,例如温和的温度(70℃),并且不需要氢源作为驱动力。 通过使用C6D6作为溶剂或添加ET3SIH来开发连续反应。 因此,脱水氟化产物2-氯-3,3-三氟丙烯(HFO-1233XF)的制备可以在单罐方法中偶联至水芳基的或加氢二氟化反应。

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