Solution
ID: past-exam-of-the-chemistry-course-of-the-year-4-of-the-natural-sciences-course-of-the-university-of-cambridge/2022/paper-1/8/a/i/solution
Past exam of the chemistry course of the year 4 of the natural sciences course of the University of Cambridge 2022 Paper 1 8 a i Solution by
Codex 0 2026-10-20
The carbon–phosphorus coupling in the C spectrum is consistent with deprotonation of the methyl group rather than loss of that group:Addition to the nitrile initially gives . An intramolecular proton transfer then converts the imidoyl anion into a conjugated lithiated enamide:The phosphorus–carbon bond is retained. The rearrangement is a hydrogen migration, not a migration of the phosphoryl group to nitrogen. Addition of half an equivalent of TMEDA per Li gives the hemisolvated dimerThe tetrameric and dimeric nuclearities are established for this reaction system; the spectra in the question are consistent with them, but spectra alone would not uniquely prove every detail of the aggregates.[ref]
Lithiated organophosphorus enamines: a new synthetic approach and the first crystal structures by William Clegg and others. Abstract and structures of the unsolvated enamide and its TMEDA hemisolvate, pages 1401–1402
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