Chemistry:Boekelheide reaction
| Boekelheide reaction | |
|---|---|
| Named after | Virgil Carl Boekelheide |
| Reaction type | Rearrangement reaction |
The Boekelheide reaction is a rearrangement of α-picoline-N-oxides to hydroxymethylpyridines. It is named after Virgil Boekelheide who first reported it in 1954.[1] Originally the reaction was carried out using acetic anhydride, which typically required a period at reflux (~140 °C). The reaction can be performed using trifluoroacetic anhydride (TFAA), which often allows for a room temperature reaction.[2]
Mechanism
The mechanism of the Boekelheide reaction begins by an acyl transfer from the trifluoroacetic anhydride to the N-oxide oxygen. The α-methyl carbon is then deprotonated by the trifluoroacetate anion. This sets the molecule up for a [3.3]-sigmatropic rearrangement which furnishes the trifluoroacetylated methylpyridine. Hydrolysis of the trifluoroacetate releases the hydroxymethylpyridine.
References
- ↑ Boekelheide, V.; Linn, W. J. (March 1954). "Rearrangements of N-Oxides. A Novel Synthesis of Pyridyl Carbinols and Aldehydes". Journal of the American Chemical Society 76 (5): 1286–1291. doi:10.1021/ja01634a026.
- ↑ Fontenas, C.; Bejan, E.; Haddou, H. Aït; Balavoine, G. G. A. (23 September 2006). "The Boekelheide Reaction: Trifluoroacetic Anhydride as a Convenient Acylating Agent". Synthetic Communications 25 (5): 629–633. doi:10.1080/00397919508011399.
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