This chapter extends the discussion to reactions between the Vilsmeier-Haack reagent (subsequently referred to as the Vilsmeier reagent for brevity) and any other compounds in which a carbon-carbon bond is formed. The discussion thus excludes reactions in which the Vilsmeier reagent acts as a chlorinating agent (for example in the preparation of acid chlorides), or in which it forms carbon-oxygen or carbon-nitrogen bonds, unless these are accompanied by formation of a carbon-carbon bond. For a discussion of the nature of the reagent and of the mechanism of the reaction, the earlier chapter in vol. 49 should be consulted. There are also a number of reviews that deal at length with mechanisms of reactions involving the Vilsmeier reagent, notably those by Jutz and Marson, and hence this chapter will concentrate on applications, with brief mention of mechanisms when necessary.



Wizinger has pointed out that alkenes could react with the Vilsmeier reagent, but his only examples were styrenes where the intermediate carbocation has considerable stability.



Hydrolysis gives the cinnamaldehyde. In principle, any alkene which is not too sterically hindered can undergo this reaction, but the Vilsmeier reagent has low reactivity as an electrophile, and in practice activation is often necessary. The addition depends on the HOMO of the alkene, and anything increasing the HOMO energy will aid reaction, as for example further conjugation (dienes, trienes, etc.) or the presence of an electron-donating substituent. Hence aldehydes and ketones are active in their enol forms, and enol ethers and enamines are good substrates. Indeed, all additions covered by this chapter can be regarded as alkene additions, even those on active methyl groups attached to electron-deficient rings. As with any reaction involving carbocation intermediates, rearrangements are possible; the initial products are sometimes enamines, and this can give rise to polysubstitution. The substrates are grouped into eleven major subsections; references to reviews of particular relevance will be found in the appropriate subsection.


Keywords:

vilsmeier reaction;
non-aromatics;
alkenes;
dienes;
polyenes;
heteroatoms;
substituents;
enamines;
enamides;
alkynes;
aldehydes;
ketones;
imines;
hydrazones;
semicarbazones;
oximes;
carboxylic acids;
anhydrides;
acid chlorides;
esters;
lactones;
amides;
lactams;
imides;
nitriles;
methyl groups;
methylene groups;
adjacent rings;
comparison of methods;
experimental conditions;
experimental procedures;
tabular survey

The Vilsmeier Reaction of Non‐Aromatic Compounds

Polycyclic N‐heterocyclic compounds. 51. Synthesis of novel 12‐substituted 11,13,15‐triazasteroidal compounds and their inhibitory activity on platelet aggregation

Polycyclic N-hetero compounds. XX: Synthesis of 11,13,15-triazasteroid with an alkyl group in the D-ring and an investigation of its antidepressive activity

Polycyclic N-hetero compounds. XLIII. Syntheses and properties of 2-substituted 1-acetoxy-6-acetyl-5,6-dihydro-4H-imidazo[1′,2′:1,6]-pyrimido[5,4-d][1]benzazepines viaN-(6,7-dihydro-5H-pyrimido[5,4-d]-[1]benzazepin-4-yl)amino acids and their analogous mesoionic compounds, and their related compounds as a series of potential blood platelet aggregation inhibitors

Polycyclic N-hetero compounds. XXXV. Syntheses and anti-platelet aggregation activity of 5,6-Dihydro-4H-benzo[3,4]cyclohept[1,2-e]imidazo[1,2-c]pyrimidines with an oxygen function at the 1-position

Polycyclic N-Hetero Compounds. XVIII. Synthesis of the 11,13,15-Triazasteroidal Skeleton with an Oxygen Function at C-17

Polycyclic N-hetero compounds. XIX. Synthesis of novel meso-ionic benz[h]imidazo[1,2-c]quinazoline and benzo[h]pyrrolo[1′,2′:3,4]imidazo[1,2-c]quinazoline derivatives

Kimiko Katsuta

Papers

Polycyclic N-Hetero Compounds. XVIII. Synthesis of the 11,13,15-Triazasteroidal Skeleton with an Oxygen Function at C-17

Polycyclic N-hetero compounds. XIX. Synthesis of novel meso-ionic benz[h]imidazo[1,2-c]quinazoline and benzo[h]pyrrolo[1′,2′:3,4]imidazo[1,2-c]quinazoline derivatives