The Blaise reaction is an organic reaction that forms a β-ketoester from the reaction of zinc metal with a α-bromoester and a nitrile.[1][2][3] The reaction was first reported by Edmond Blaise (1872–1939) in 1901. The final intermediate is a metaloimine, which is then hydrolyzed to give the desired β-ketoester.[4]
| Blaise reaction | |
|---|---|
| Named after | Edmond E. Blaise |
| Reaction type | Coupling reaction |
| Identifiers | |
| Organic Chemistry Portal | blaise-reaction |
| RSC ontology ID | RXNO:0000237 |
Bulky aliphatic esters tend to give higher yields. Steven Hannick and Yoshito Kishi have developed an improved procedure.[5]
It has been noted[6][7] that free hydroxyl groups can be tolerated in the course of this reaction, which is surprising for reactions of organometallic halides.
Mechanism
editThe mechanism of the Blaise reaction involves the formation of an organozinc complex with the bromine alpha to the ester carbonyl. This makes the alpha carbon nucleophilic, allowing it to attack the electrophilic carbon of the nitrile. The negative nitrile nitrogen resulting from this attack complexes with the zinc monobromide cation. The β-enamino ester (tautomer of the imine intermediate pictured above) product is revealed by work-up with 50% K2CO3 aq. If the β-ketoester is the desired product, addition of 1 M hydrochloric acid hydrolyzes the β-enamino ester to turn the enamino into a ketone, forming the β-ketoester.
See also
editReferences
edit- ^ Edmond E. Blaise; Compt. Rend. 1901, 132, 478.
- ^ Rinehart, K. L., Jr. Organic Syntheses, Coll. Vol. 4, p. 120 (1963); Vol. 35, p. 15 (1955). (Article)
- ^ Rao, H. S. P.; Rafi, S.; Padmavathy, K. Tetrahedron 2008, 64, 8037-8043. (Review)
- ^ Cason, J.; Rinehart, K. L., Jr.; Thorston, S. D., Jr. J. Org. Chem. 1953, 18, 1594. (doi:10.1021/jo50017a022)
- ^ Hannick, S. M.; Kishi, Y. J. Org. Chem. 1983, 48, 3833. (doi:10.1021/jo00169a053)
- [8] Marko, I.E. J. Am. Chem. Soc. 2007, ASAP doi:10.1021/ja0691728
- [9] Wang, D.; Yue, J.-M. Synlett 2005, 2077-2079.