Van Leusen reaction

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Van Leusen reaction
Named after Daan Van Leusen
Albert M. Van Leusen
Reaction type Substitution reaction
Reaction
ketone
+
TosMIC
nitrile
Identifiers
Organic Chemistry Portal van-leusen-reaction

The Van Leusen reaction is the reaction of a ketone with TosMIC leading to the formation of a nitrile. It was first described in 1977 by Van Leusen and co-workers.[1] When aldehydes are employed, the Van Leusen reaction is particularly useful to form oxazoles and imidazoles.

drawing of the van leusen reaction
drawing of the van leusen reaction

Mechanism

The

carbonyl is followed by 5-endo-dig cyclisation (following Baldwin's rules
) into a 5-membered ring.

Van Leusen oxazole synthesis
Named after Daan Van Leusen
Albert M. Van Leusen
Reaction type Ring forming reaction
Reaction
aldehyde
oxazole
Identifiers
Organic Chemistry Portal van-leusen-oxazole-synthesis

If the substrate is an aldehyde, then

can occur readily. Upon quenching, the resulting molecule is an oxazole.

Van Leusen imidazole synthesis
Named after Daan Van Leusen
Albert M. Van Leusen
Reaction type Ring forming reaction
Identifiers
Organic Chemistry Portal van-leusen-imidazole-synthesis

If an

aldimine is used, formed from the condensation of an aldehyde with an amine, then imidazoles can be generated through the same process.[2]

Mechanism showing the synthesis of an oxazole through the Van Leusen reaction
Mechanism showing the synthesis of an oxazole through the Van Leusen reaction

When ketones are used instead, elimination cannot occur; rather, a

tautomerization
process gives an intermediate which after a ring opening process and elimination of the tosyl group forms an N-formylated alkeneimine. This is then solvolysed by an acidic alcohol solution to give the nitrile product.

Mechanism for the Van Lausen reaction
Mechanism for the Van Lausen reaction

References