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Alkyl aldehydes

In 1883, Bottinger described the reaction of aniline and pyruvic acid to yield a methylquinolinecarboxylic acid. He found that the compound decarboxylated and resulted in a methylquinoline, but made no effort to determine the position of either the carboxylic acid or methyl group. Four years later, Doebner established the first product as 2-methylquinoline-4-carboxylic acid (8) and the second product as 2- methylquinoline (9). Under the reaction conditions (refluxing ethanol), pyruvic acid partially decarboxylates to provide the required acetaldehyde in situ. By adding other aldehydes at the beginning of the reaction, Doebner found he was able to synthesize a variety of 2-substituted quinolines. While the Doebner reaction is most commonly associated with the preparation of 2-aryl quinolines, in this primary communication Doebner reported the successful use of several alkyl aldehydes in the quinoline synthesis. [Pg.407]

For aromatic amines, the reaction is very general. Halogen, nitro, alkyl, aldehyde, sulfonic acid, and so on, groups do not interfere. Since aliphatic amines do not react with nitrous acid below a pH of 3, it is even possible, by working at a pH of 1, to diazotize an aromatic amine without disturbing an aliphatic amino group in the same molecule. ... [Pg.816]

The present homoallylation with isoprene under Ni-Et3B catalysis shows marginal success for the reaction with aliphatic aldehydes. Results are summarized in Table 6. Primary alkyl aldehydes (bearing no a-substituents) and sterically less-hindered secondary alkyl aldehydes undergo the homoallylation successfully to provide the expected products in good yields with excellent stereoselectivity (runs 1-5). The results in runs 3-5 indicate that the present reaction shows almost no diastereofacial selectivity with respect to the a-stereo centers of secondary alkyl aldehydes. Sterically demanding aldehydes, such as cyclohexanecarbaldehye and pivalaldehyde, provide the... [Pg.196]

Optically active /3-ketoiminato cobalt(III) compounds based on chiral substituted ethylenedi-amine find use as efficient catalysts for the enatioselective hetero Diels Alder reaction of both aryl and alkyl aldehydes with l-methoxy-(3-(t-butyldimethylsilyl)oxy)-1,3-butadiene.1381 Cobalt(II) compounds of the same class of ligands promote enantioselective borohydride reduction of ketones, imines, and a,/3-unsaturated carboxylates.1382... [Pg.118]

One of the important new directions in the study of addition reactions of organozinc compounds to aldehydes is the use of ionic liquids. Usually, application of these compounds in reactions with common organometallic reagents has a serious problem ionic solvents are usually reactive toward them, particularly Grignard and organolithium derivatives. It has been recently reported that carbonyl compounds react with allylzinc bromide formed in situ from allyl bromide and zinc in the ionic liquid 3-butyl-l-methylimidazolium tetrafluoroborate, [bmim][BF4].285 Another important finding is that the more reactive ZnEt2 alkylates aldehydes in a number of ionic liquids at room temperature.286 The best yields (up to 96%) were obtained in A-butylpyridinium tetrafluoroborate, [bpy][BF4] (Scheme 107). [Pg.387]

The 10-57-5-hydridosiliconate ion 62 is known in association with lithium,323 tetrabutylammonium,101 and bis(phosphoranyl)iminium93 cations. It is synthesized by hydride addition to the 8-.S7-4-silane 63, which is derived from hexafluoroacetone.101 Benzaldehyde and related aryl aldehydes are reduced by solutions of 62 in dichloromethane at room temperature101 or in tetrahydrofuran at 0°96 within two hours. The alkyl aldehyde, 1-nonanal, is also reduced by 62 in tetrahydrofuran at O0.96 Good to excellent yields of the respective alcohols are obtained following hydrolytic workup. The reactions are not accelerated by addition of excess lithium chloride,96 but neutral 63 catalyzes the reaction, apparently through complexation of its silicon center with the carbonyl oxygen prior to delivery of hydride from 62.101... [Pg.62]

They offer the advantage that reductions can be effected under conditions that permit the conversion of substrates that may be adversely sensitive to the presence of strong Brpnsted acids. For example, in the presence of a 10% excess of triethylsilane, addition of one-half equivalent of boron trifluoride etherate to octanal results, within one hour, in the formation of a 66% yield of dioctyl ether after a basic hydrolytic workup. Benzaldehyde provides a 75% yield of dibenzyl ether under the same reaction conditions. The remainder of the mass is found as the respective alcohol.70 Zinc chloride is also capable of catalyzing this reaction. With its use, simple alkyl aldehydes are converted into the symmetrical ethers in about 50% yields.330... [Pg.66]

Fig. 11.4. Electron ionization mass spectrum of nonanal. Unlike the previous example (toluene, Fig. 11.3), this 9-carbon alkyl aldehyde displays extensive fragmentation and a very low abundance molecular ion at mlz 142. The extensive degree of fragmentation exhibited by many compounds under El conditions makes manual interpretation complex and tedious. Consequently, computerized searches of spectral libraries find extensive use in compound identification. Fig. 11.4. Electron ionization mass spectrum of nonanal. Unlike the previous example (toluene, Fig. 11.3), this 9-carbon alkyl aldehyde displays extensive fragmentation and a very low abundance molecular ion at mlz 142. The extensive degree of fragmentation exhibited by many compounds under El conditions makes manual interpretation complex and tedious. Consequently, computerized searches of spectral libraries find extensive use in compound identification.
The second category of aldehyde dehydrogenases are efficient catalysts of the oxidation of both aryl and alkyl aldehydes to the corresponding carboxylic acids. The most well known and common of such reactions is the oxidation of acetaldehyde, derived from alcohol, to acetic acid. [Pg.61]

Rate constants and Arrhenius parameters for the reaction of Et3Si radicals with various carbonyl compounds are available. Some data are collected in Table 5.2 [49]. The ease of addition of EtsSi radicals was found to decrease in the order 1,4-benzoquinone > cyclic diaryl ketones, benzaldehyde, benzil, perfluoro propionic anhydride > benzophenone alkyl aryl ketone, alkyl aldehyde > oxalate > benzoate, trifluoroacetate, anhydride > cyclic dialkyl ketone > acyclic dialkyl ketone > formate > acetate [49,50]. This order of reactivity was rationalized in terms of bond energy differences, stabilization of the radical formed, polar effects, and steric factors. Thus, a phenyl or acyl group adjacent to the carbonyl will stabilize the radical adduct whereas a perfluoroalkyl or acyloxy group next to the carbonyl moiety will enhance the contribution given by the canonical structure with a charge separation to the transition state (Equation 5.24). [Pg.101]

IrCl2H(cod)]2 catalyzed the synthesis of substituted quinolines, where the reachon of aniline derivahves, aromatic and alkyl aldehydes efficiently proceeds under an oxygen atmosphere (Scheme 11.34) [46]. The plausible mechanism consists of a Mannich reaction, a Friedel-Craft-type aromahc substituhon, dehydration, and dehydrogenation. This can be recognized as a formal [4+2] cycloaddition of N-aryl imine and enol (Scheme 11.35). [Pg.292]

Finally, addition of the carbanions derived from 83 to non-enolizable aldehydes is a facile process. Aryl and tertiary alkyl aldehydes gave trimethylsilyl allyl ethers 85 by a [1,4]-Brook isomerization (equation 30). The stereochemistry of the intermediate alkoxides 84 dramatically influences the reaction conditions required . [Pg.472]

Excellent enantioselectivities up to complete asymmetric induction are achieved in the preparation of a-alkylated aldehydes, acyclic and cyclic ketones via (-)-(S)- and (+ )-(7 )-1 -amino-2-methoxymethylpyrrolidine (SAMP/RAMP-hydrazones) (see Section 1.1.1.4.2.). Due to the unique mechanism of metalation and alkylation, the absolute configuration of the final products can be predicted. Since both antipodes of the auxiliary are available, either enantiomer of the desired alkylated carbonyl compound can be prepared... [Pg.972]

Table 5. a-Alkylated Aldehydes by Alkylation of Chiral Aldimines, Followed by Hydrolysis2... [Pg.986]

In addition, alkylated aldehydes can be transformed to (—)-(5)-l-amino-2-(tcr/-butyldi-methylsilyloxymethyl)pyrrolidine (SASP)-hydrazones without racemization. The diastereomeric ratio of these hydrazones can be determined directly using HPLC. Furthermore, this method allows determination of the absolute configuration of the alkylated hydrazones, since SASP-hy-drazones of (S, -configuration always elute first11 25. [Pg.1012]

Reduction of alkylated aldehyde-derived SAMP-hydrazones, followed by reductive N —N cleavage of the resulting hydrazines with Raney nickel, furnishes /(-substituted primary amines in good chemical yields and without racemization in 94-99% ee (see Table 5)31. [Pg.1013]

Recent work by several groups has shown that formation of oxetanes from alkyl aldehydes and ketones can take place from the singlet as well as from the triplet state.66... [Pg.256]

Transition State Models. The stoichiometry of aldehyde, dialkylzinc, and the DAIB auxiliary strongly affects reactivity (Scheme 9) (3). Ethylation of benzaldehyde does not occur in toluene at 0°C without added amino alcohol however, addition of 100 mol % of DAIB to diethylzinc does not cause the reaction either. Only the presence of a small amount (a few percent) of the amino alcohol accelerates the organometallic reaction efficiently to give the alkylation product in high yield. Dialkyl-zincs, upon reaction with DAIB, eliminate alkanes to generate alkylzinc alkoxides, which are unable to alkylate aldehydes. Instead, the alkylzinc alkoxides act as excellent catalysts or, more correctly, catalyst dimers (as shown below) for reaction between dialkylzincs and aldehydes. The unique dependence of the reactivity on the stoichiometry indicates that two zinc atoms per aldehyde are responsible for the alkyl transfer reaction. [Pg.141]

As described in Scheme 25, the first method starts with the conversion of an a-amino acid into a p-amino-p-alkyl aldehyde. Then, the chiral aldol condensation between the resulting aldehyde and an oxazolidinone derivative is carried out. In the last step, removal of the oxazolidinone provides the desired product. [Pg.388]

Riec ne St Meister for polymeric peioudes derived from alkyl aldehydes or alkyl ketones. They assigned to them the formulae ... [Pg.131]

The synthesis of racemic a-alkyl aldehydes by this method is feasible, although recourse to the methods previously described may be more convenient, as formulated below. [Pg.601]


See other pages where Alkyl aldehydes is mentioned: [Pg.22]    [Pg.45]    [Pg.37]    [Pg.38]    [Pg.293]    [Pg.341]    [Pg.113]    [Pg.233]    [Pg.69]    [Pg.72]    [Pg.436]    [Pg.560]    [Pg.184]    [Pg.95]    [Pg.172]    [Pg.222]    [Pg.232]    [Pg.41]    [Pg.16]    [Pg.215]    [Pg.350]    [Pg.985]    [Pg.1006]    [Pg.49]    [Pg.260]    [Pg.22]    [Pg.494]    [Pg.510]   
See also in sourсe #XX -- [ Pg.411 ]




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Aldehydes, alkylation

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