Ruthenium-catalyzed selective α-deuteration of aliphatic nitriles using D2O.

Ruthenium-catalyzed selective α-deuteration of aliphatic nitriles using D2O.
Chem Commun (Camb). 2018 Jul 19;:
Authors: Krishnakumar V, Gunanathan C
Abstract
Selective catalytic α-deuteration of aliphatic nitriles using deuterium oxide as a deuterium source is reported. A PNP-ruthenium pincer complex catalyzed the α-deuteration of aliphatic nitriles including acetonitrile. Efficient deuteration occurred with a low catalyst load (0.2 to 0.5 mol%) and under mild conditions. A [2+2] cycloadduct formation from nitrile functionality and a deprotonated catalytic intermediate, followed by an imine-enamine tautomerization and a H/D exchange between the enamine intermediate and deuterium oxide leading to the selective deuteration at the α-position of the nitrile, is proposed as a plausible reaction mechanism.
PMID: 30022195 [PubMed - as supplied by publisher]

Source: Chemical Communications - July 19, 2018 Category: Chemistry Authors: Krishnakumar V, Gunanathan C Tags: Chem Commun (Camb) Source Type: research