Modular synthesis of 2-furyl carbinols from 3-benzyl-dimethylsilylfurfural platforms relying on oxygen-assisted C-Si bond functionalization

3-Silylated furfurals, readily prepared in three steps from biomass-derived furfural and 5-methylfurfural, are converted into 3-sily-lated 2-furyl carbinols upon condensation with organomagnesium or organolithium reagents. The hydroxy unit of the carbinol adducts can be exploited to promote C3(sp(2))-Si bond functionalization through intramolecular activation. Two approaches were contemplated for this purpose. Activation by alkoxides of the C3-SiEt3 or C3-SiMe(2)t-Bu bonds was ineffective. Conversely, treat-ment of the C3-benzyldimethylsilyl-appended derivatives with tetrabutylammonium fluoride led to cyclic siloxanes, which revealed to be competent donors for copper-catalyzed cross-coupling reactions, such as arylation reactions catalyzed by Pd-2(dba)(3)/CuI, as well as allylation and methylation reactions catalyzed by CuI.PPh3. C3-Benzyldimethylsilyl-appended furfurals are thus introduced as versatile platforms, providing a modular access to 3-substituted 2-furyl carbinols from renewable feedstock.

Automated summary

3-silylated furfurals are converted into 3-silylated 2-furyl carbinols upon condensation with organomagnesium or organolithium reagents. The hydroxy unit of the carbinol adducts can be exploited to promote C3(sp(2))-Si bond functionalization through intramolecular activation. This study introduces versatile platforms for the synthesis of 3-substituted 2-furyl carbinols from renewable feedstock.