Stephen aldehyde synthesis

Stephen aldehyde synthesis, a named reaction in chemistry, was invented by Henry Stephen (OBE/MBE). This reaction involves the preparation of aldehydes (R-CHO) from nitriles (R-CN) using tin(II) chloride (SnCl2), hydrochloric acid (HCl) and quenching the resulting iminium salt ([R-CH=NH2]+Cl−) with water (H2O).[1][2] During the synthesis, ammonium chloride is also produced.

Stephen aldehyde synthesis
Not to be confused with Stevens rearrangement.
Stephen aldehyde synthesis
Named after Henry Stephen
Reaction type Organic redox reaction

Mechanism

The following scheme shows the reaction mechanism:

Stephen aldehyde synthesis: Reaction mechanism

By addition of hydrogen chloride the used nitrile (1) reacts to its corresponding salt (2). It is believed that this salt is reduced by a single electron transfer by the tin(II) chloride (3a and 3b).[3] The resulting salt (4) precipitates after some time as aldimine tin chloride (5). Hydrolysis of 5 produces an amide (6) from which an aldehyde (7) is formed.

Substitutes that increase the electron density promote the formation of the aldimin-tin chloride adduct. By electron withdrawing substituents, the formation of amide chloride is facilitated.[4] In the past, the reaction was carried out by precipitating the aldimine-tin chloride, washing it with ether and then hydrolyzing it. However, it has been found that this step is unnecessary and the aldimine tin chloride can be hydrolysed directly in the solution.[5]

This reaction is more efficient when aromatic nitriles are used instead of aliphatic ones. However, even for some aromatic nitriles (e. g. 2-formylbenzoic acid ethyl ester) the yield can be low.[5]

Sonn-Müller method

In the Sonn-Müller method[6][7] the intermediate iminium salt is obtained from reaction of an amide PhCONHPh with phosphorus pentachloride.

See also

References
  1. Williams, Jonathan W. (1943). "β-Naphthaldehyde". Organic Syntheses. 23: 63. doi:10.15227/orgsyn.023.0063.
  2. Stephen, Henry. (1925). "A new synthesis of aldehydes". J. Chem. Soc., Trans. 127: 1874–1877. doi:10.1039/CT9252701874.
  3. Wang, Zerong (2009). Comprehensive Organic Name Reactions and Reagents, 3 Volume Set. John Wiley & Sons, Hoboken, New Jersey. pp. 2659–2660. ISBN 978-0-471-70450-8.
  4. Rabinovitz, Mordecai (1970). "Chapter 7. Reduction of the cyano group". In Rappoport, Zvi (ed.). The Cyano group (1970). PATAI'S Chemistry of Functional Groups. John Wiley & Sons, Ltd., Chichester, UK. p. 308. doi:10.1002/9780470771242.ch7. ISBN 978-0-470-77124-2.
  5. Wang, Zerong (2009). Comprehensive Organic Name Reactions and Reagents, 3 Volume Set. John Wiley & Sons, Hoboken, New Jersey. pp. 2659–2660. ISBN 978-0-471-70450-8.
  6. Adolf, Sonn; Müller, Ernst (1919). "Über eine neue Methode zur Umwandlung von Carbonsäuren in Aldehyde" [About a new method for converting carboxylic acids into aldehydes]. Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 52 (10): 1927–1934. doi:10.1002/cber.19190521002.
  7. Williams, Jonathan W.; Witten, Charles H.; Krynitsky, John A. (1946). "o-Tolualdehyde". Organic Syntheses. 26: 97. doi:10.15227/orgsyn.026.0097.
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