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A synthetic protocol has been developed for the gram-scale synthesis of 4,4,4-trifluorobut-2-ynal based on the commercially available, environmentally friendly fourth-generation refrigerant HFO-1234yf (2,3,3,3-tetrafluoropropene). The synthesis comprises the three following stages: obtaining 3,3,3-trifluoropropyne, its transformation into 4,4-diethoxy-1,1,1-trifluorobut-2-yne via the Bodroux-Chichibabin reaction, and subsequent hydrolysis of the latter compound, giving the final 4,4,4-trifluorobut-2-ynal. The proposed protocol expands the synthetic potential of CF3-alkynes by providing preparative availability for an original organofluorine substance.
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LISNIK et al. (2026) studied this question.
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