Selective α-Deuteration of Cinnamonitriles using D2O as Deuterium Source

Beibei Guo, Johannes G. de Vries*, Edwin Otten*

*Bijbehorende auteur voor dit werk

OnderzoeksoutputAcademicpeer review

1 Citaat (Scopus)
100 Downloads (Pure)

Samenvatting

The selective α-deuteration of α,β-unsaturated nitriles using the strong base tBuOK or a metal-ligand cooperative Ru pincer catalyst is described. With D2O as deuterium source and glyme as solvent at 70 °C, tBuOK is an efficient catalyst for deuteration at the α-C(sp 2) position of cinnamonitriles, providing access to a broad range of deuterated derivatives in good to excellent yields and with very high levels of deuterium incorporation. While the tBuOK-catalysed protocol does not tolerate base-sensitive functional groups, cinnamonitrile derivatives containing a benzylic bromide or ester moiety were deuterated in excellent yields using Milstein's ruthenium PNN pincer catalyst. Moreover, the activity for H/D exchange of the metal-ligand cooperative Ru catalyst is found to be significantly higher than that of tBuOK, allowing reactions to proceed well even at room temperature. A mechanistic proposal is put forward that involves deprotonation of the cinnamonitrile α-CH position when using tBuOK as catalyst, whereas H/D exchange catalysis with the Ru PNN pincer likely proceeds via (reversible) oxa-Michael addition of D2O.

Originele taal-2English
Pagina's (van-tot)179-186
Aantal pagina's8
TijdschriftAdvanced Synthesis and Catalysis
Volume364
Nummer van het tijdschrift1
Vroegere onlinedatum27-sep.-2021
DOI's
StatusPublished - 4-jan.-2022

Vingerafdruk

Duik in de onderzoeksthema's van 'Selective α-Deuteration of Cinnamonitriles using D2O as Deuterium Source'. Samen vormen ze een unieke vingerafdruk.

Citeer dit