Combining two or more consecutive reactions in one pot is a common approach for process development, as such a method involves cheap starting materials and allows generation of a reactive intermediate, to undergo further reaction, without isolation. Herein, we report the synthesis of a vinylene-linked (-CH═CH-) covalent organic framework, COF-701, directly from acetonitrile, a cheap commodity solvent, by combining/telescoping two consecutive reactions-cyclotrimerization of nitrile and subsequent aldol condensation with aldehydes-in one pot. Acetonitrile is trimerized to generate protonated 2,4,6-trimethyl-s-triazine tautomers , which undergo Aldol condensation with 4,4'-biphenyldicarbaldehyde in one pot to form crystalline COF-701.
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