# Chemoselectivity - Hydrogenation¶

Reagent Name Function
$$\ce{-H2, Pd/C}$$ in $$\ce{MeOH}$$ or $$\ce{EtOH}$$ at $$75^\circ C$$ Palladium on carbon mild - won’t hydrogenate aromatics
$$\ce{RC#CR -> H2RC-CRH2}$$ $$\ce{}$$
$$\ce{R2C=CR2 -> HR2C-CR2H}$$
$$\ce{OR -> OH}$$
$$\ce{NR_{x} -> NH_{x}}$$
$$\ce{-H2, Pd/BaSO4}$$ Reagents for the Rosenmund Reaction deactivating substrate
$$\ce{-H2, Pd/CaCO3, Pb(OAc)2}$$ Lindlar’s catalyst deactivating substrate and $$\ce{Pb(OAc)2}$$
alkyne → alkene (→ alkane is very slow)
$$\ce{-H2, PtO2}$$ in $$\ce{AcOH}$$ at $$25^\circ C$$ Adam’s catalyst aromatics → cyclic alkane
$$\ce{-H2, Ni}$$ at $$50^\circ C, 100\:atm$$ aromatics → cyclic alkane
Substrate Usual choice of metal
Benzyl amine or ether (protecting groups) Pd
Alkene Pd, Pt, or Ni
Aromatic ring Pt, or Rh, or Ni under pressure

## Surface Catalytic Hydrogenation¶

the process of catalytic hydrogenation is different to nucleophilic reducing agents in that it takes place on the surface of metal particles. The metal particles are finely divided and mixed with a support.

Note

Since it is a surface catalytic process, the products will be on the same face (syn configuration).

## Hydrogenation of alkenes¶

This is pretty simply done with palladium on carbon (Pd/C)

And will work on cyclic structures as well as linear ones

## Hydrogenation of Aromatic Rings¶

Stronger catalysts will also be able to hydrogenate aromatic rings to cyclic alkanes, such as nickel under pressure, or $$\ce{PtO2}$$

## Hydrogenation of Acyl chlorides → Aldehydes (Rosenmund Reaction)¶

Acyl chlorides are really easy to hydrogenate, so to ensure that nothing else is reacted, we can use the $$\ce{BaSO4}$$ support which will allow the products to escape before being over-reduced to an alcohol. It is a deactivating substrate.

## Alkyne → Alkene (Lindlar’s Catalyst)¶

Lindlar’s catalyst is selective for the alkyne to alkene hydrogenation. Alkenes are typically easily hydrogenated to alkanes, but the reagent is on a deactivating substrate, as well as being “poisoned” with the lead. This causes the reduction form alkene → alkane to be manageably slow.

## Hydrogenolysis of Benzyl Ethers and Amines (Protecting Groups)¶

Protecting groups are useful for ensuring that only the correct groups will react, however once the reaction is done, they need to be lysed back to their intended form. In this case, back to a tertiary alcohol and secondary amine