Despite its unique structure and potential use as an important building block in organic synthesis, the title alpha-oxoketene 1 has been formed mostly under very special conditions as a short-lived species. The reactivity of 1 is, therefore, nearly unexplored. In great contrast, it seemed that its ionized gaseous form 1*+ is stable and easily accessible. In this study, we used multiple-stage pentaquadrupole mass spectrometry to probe the formation of gaseous 1*+ and explore its stability and intrinsic reactivity. With water and methanol, gaseous 1*+ was found to react similarly to solvated 1, which indicates that there is a close parallel between their reactivities. Gaseous 1*+ was also found to react promptly via polar [3 + 2] cycloadditons with various dienophiles including alkenes, alkynes, isocyanates, ketones and esters, thus forming a series of benzopyran-4-ones (flavones, 4-chromanones, 4-chromenones, benzo[1,3]dioxin-4-ones, and analogues) that are common structural units in many natural products. The present availability of 1 at room temperature and the gas-phase findings reported herein for gaseous 1*+ indicate that solvated 1 should undergo many [4 + 2] cycloadditions and functions as a versatile precursor of a variety of biologically active molecules.
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