Journal of Fluorine Chemistry ( IF 1.7 ) Pub Date : 2019-04-03 , DOI: 10.1016/j.jfluchem.2019.04.001 Maëva-Charlotte Kervarec , Clara Patricia Marshall , Thomas Braun , Erhard Kemnitz
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 CF bond was observed, under remarkable conditions, such as mild temperatures (70 °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.
中文翻译:
使用纳米级氟化铝催化剂在温和条件下将2-氯-1,1,1,2-四氟丙烷(HCFC-244bb)选择性脱氟化氢为2-氯-3,3,3-三氟丙烯(HFO-1233xf)
测试了氯氟化铝(ACF,AlCl x F 3-x,x = 0.05-0.3)和高表面氟化铝(HS -AlF 3)作为多相催化剂对2-氯-1,1,1,2的反应性-四氟丙烷(HCFC-244bb),这是一种有力的温室气体。在诸如温和的温度(70°C)等显着条件下并且不需要氢源作为驱动力的情况下,观察到C F键的选择性活化和脱氢氟化作用。通过使用C 6 D 6作为溶剂或添加Et 3进行连续反应SiH。因此,脱氢氟化产物2-氯-3,3,3-三氟丙烯(HFO-1233xf)的生产可以通过一锅法与加氢芳基化或加氢脱氟反应偶联。