How could you go from an nitrile to an aldehyde without using acidic conditions? for example to keep an acetal group intact? 1)LAH, 2) PCC or 1)SOCl2, 2) LiAl(t-BuO)3H are options but i'm not sure if they require acidic workup or if water works aswell.
Can you do the full story of happens with the complex part please! How do you get rid of AlH2 and how does nitrogen get h2
How could you go from an nitrile to an aldehyde without using acidic conditions? for example to keep an acetal group intact? 1)LAH, 2) PCC or 1)SOCl2, 2) LiAl(t-BuO)3H are options but i'm not sure if they require acidic workup or if water works aswell.
thannnk you
Also stephans reduction would reduce CN to CHO.
Thanks