Étard reaction

Étard reaction
Named after	Alexandre Léon Étard
Reaction type	Organic redox reaction
Identifiers
Organic Chemistry Portal	étard-reaction

The Étard reaction is a chemical reaction that involves the direct oxidation of an aromatic or heterocyclic bound methyl group to an aldehyde using chromyl chloride.^[1]^[2]^[3] For example, toluene can be oxidized to benzaldehyde.

It is named for the French chemist Alexandre Léon Étard (5 January 1852, Alençon – 1 May 1910).

Reaction mechanism

The reaction mechanism proceeds via an ene reaction with chromyl chloride, forming the precipitated Étard complex. The Étard complex is then decomposed by a [2,3] sigmatropic rearrangement under reducing conditions to prevent further oxidation to a carboxylic acid. Reducing conditions for the decomposition of the Étard complex are provided by saturated aqueous sodium sulphite. Typical solvents for the reaction include carbon disulfide, dichloromethane,^[4] chloroform, and carbon tetrachloride, with carbon tetrachloride being the most common. To obtain a highly purified aldehyde product, the Étard complex precipitate is often purified before decomposition in order to prevent reaction with any unreacted reagent. The reaction is normally carried out for a few days to several weeks and the yields are high.^[5]^[6]

Limitations

The Étard reaction is most commonly used as a relatively easy method of converting toluene into benzaldehyde. Obtaining specific aldehyde products from reagents other than toluene tends to be difficult due to rearrangements. For example, n-propylbenzene is oxidized to propiophenone, benzyl methyl ketone, and several chlorinated products, with benzyl methyl ketone being the major product.^[7]^[8] Another example arises from the Étard reaction of trans-decalin which results in a mixture of trans-9-decalol, spiro [4.5]decan-6-one, trans-1-decalone, cis-1-decalone, 9,10-octal-1-one, and 1-tetralone.^[9]

Other oxidation reagents like potassium permanganate or potassium dichromate oxidize to the more stable carboxylic acids.

Uses

Oxidation of toluene to benzaldehyde is quite a useful conversion. Benzaldehyde is routinely used for its almond flavor. The aldehyde is comparatively reactive and readily participates in aldol condensations. Benzaldehyde can serve as a precursor for various compounds, including dyes, perfumes, and pharmaceuticals. For example, the first step in the synthesis of ephedrine is condensation of benzaldehyde with nitroethane ^{[citation needed]}. Additionally, benzaldehyde is instrumental in the synthesis of phentermine.^[10] Unlike other oxidising agents (like KMnO₄ or CrO₃ etc.), chromyl chloride does not oxidise aldehyde to carboxylic acid.

References

^ Étard, A. (1880). "Sur la synthèse desaldéhydes aromatiques; essence de cumin" [On the synthesis of aromatic aldehydes ; essence of cumin]. Comptes Rendus Hebdomadaires des Séances de l'Académie des Sciences (in French). 90: 534. Archived from the original on 1 March 2012.
^ Étard, A. (1881). "Recherches sur le rôle oxydant de l'acide chlorochromique". Annales de Chimie et de Physique (in French). 22: 218–286. Archived from the original on 1 March 2012.
^ Hartford, W. H. & Darrin, M. (1958). "The Chemistry Of Chromyl Compounds". Chemical Reviews. 58: 1–61. doi:10.1021/cr50019a001.
^ F. Freeman (2004). "Chromyl Chloride". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rc177. ISBN 0471936235.
^ Necsoiu, I.; Balaban, A. T.; Pascaru, I.; Sliam, E.; Elian, M.; Nenitzescu, C. D. (1963). "The mechanism of the Étard reaction". Tetrahedron. 19 (7): 1133–1142. doi:10.1016/s0040-4020(01)98572-2.
^ Wheeler, Owen H. (1958). "Étard Reaction: I. Its Scope and Limitation with Substituted Toluenes". Canadian Journal of Chemistry. 36 (4): 667–670. doi:10.1139/v58-093.
^ Renţea, C. N.; Necşoiu, I.; Renţes, M.; Ghenciulescu, A. & Nenitzescu, C. D. (1966). "Étard reaction—III: Oxidation of N-propylbenzene and methylcyclohexane with chromyl chloride". Tetrahedron. 22 (10): 3501–3513. doi:10.1016/s0040-4020(01)92538-4.
^ Wiberg, K. B.; Marshall, B. & Foster, G. (1962). "Some observations on the Étard reaction". Tetrahedron Letters. 3 (8): 345–348. doi:10.1016/s0040-4039(00)70878-1.
^ Renţea, C. N.; Renţea, M.; Necşoiu, I. & Nenitzescu, C. D. (1968). "Étard reaction—VI: Oxidation of cis and trans-decaline with chromyl chloride". Tetrahedron. 24 (13): 4667–4676. doi:10.1016/s0040-4020(01)98663-6.
^ Vardanyan, Ruben S. & Hruby, Victor J. (2006). Synthesis of Essential Drugs (first ed.). Amsterdam: Elsevier Science. ISBN 978-0-444-52166-8.

[1] Étard, A. (1880). "Sur la synthèse desaldéhydes aromatiques; essence de cumin" [On the synthesis of aromatic aldehydes ; essence of cumin]. Comptes Rendus Hebdomadaires des Séances de l'Académie des Sciences (in French). 90: 534. Archived from the original on 1 March 2012.

[2] Étard, A. (1881). "Recherches sur le rôle oxydant de l'acide chlorochromique". Annales de Chimie et de Physique (in French). 22: 218–286. Archived from the original on 1 March 2012.

[3] Hartford, W. H. & Darrin, M. (1958). "The Chemistry Of Chromyl Compounds". Chemical Reviews. 58: 1–61. doi:10.1021/cr50019a001.

[4] F. Freeman (2004). "Chromyl Chloride". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rc177. ISBN 0471936235.

[5] Necsoiu, I.; Balaban, A. T.; Pascaru, I.; Sliam, E.; Elian, M.; Nenitzescu, C. D. (1963). "The mechanism of the Étard reaction". Tetrahedron. 19 (7): 1133–1142. doi:10.1016/s0040-4020(01)98572-2.

[6] Wheeler, Owen H. (1958). "Étard Reaction: I. Its Scope and Limitation with Substituted Toluenes". Canadian Journal of Chemistry. 36 (4): 667–670. doi:10.1139/v58-093.

[7] Renţea, C. N.; Necşoiu, I.; Renţes, M.; Ghenciulescu, A. & Nenitzescu, C. D. (1966). "Étard reaction—III: Oxidation of N-propylbenzene and methylcyclohexane with chromyl chloride". Tetrahedron. 22 (10): 3501–3513. doi:10.1016/s0040-4020(01)92538-4.

[8] Wiberg, K. B.; Marshall, B. & Foster, G. (1962). "Some observations on the Étard reaction". Tetrahedron Letters. 3 (8): 345–348. doi:10.1016/s0040-4039(00)70878-1.

[9] Renţea, C. N.; Renţea, M.; Necşoiu, I. & Nenitzescu, C. D. (1968). "Étard reaction—VI: Oxidation of cis and trans-decaline with chromyl chloride". Tetrahedron. 24 (13): 4667–4676. doi:10.1016/s0040-4020(01)98663-6.

[10] Vardanyan, Ruben S. & Hruby, Victor J. (2006). Synthesis of Essential Drugs (first ed.). Amsterdam: Elsevier Science. ISBN 978-0-444-52166-8.

[1]

[2]

[3]

[4]

[5]

[6]

[7]

[8]

[9]

[10]

Agama	Bahasa	Biografi	Budaya	Ekonomi	Elektronika
Film	Filsafat	Geografi	Indonesia	Ilmu	Lingkungan
Masyarakat	Matematika	Militer	Mitologi	Musik	Olahraga
Pendidikan	Politik	Sastra	Sejarah	Seni	Teknologi

Étard reaction

Reaction mechanism

Limitations

Uses

References

Read other articles:

Ezzard Charles

ملعب هاسيلي كروفورد

Daftar kabupaten dan kota di Papua Selatan

The Hill (surat kabar)

KLIX-FM

The Calculating Stars

Hoplocerambyx severus

أحمد قريع

Liste des sénateurs des États-Unis pour le Wyoming

Синелобый амазон

Gilyanov

Halo (religious iconography)

Chancelier de France

طواف بولندا 2023

大字 (数字)

Lecco Calcio 1977-1978

Revolutionary Left Movement (Chile)

Walker River

克瓦米·恩克鲁玛

Ich will

Portal di Ensiklopedia Dunia