Salts quaternary ammonium fluoride

Nitroarenes are reduced to anilines (>85%) under the influence of metal carbonyl complexes. In a two-phase system, the complex hydridoiron complex [HFe,(CO)u]2-is produced from tri-iron dodecacarbonyl at the interface between the organic phase and the basic aqueous phase [7], The generation of the active hydridoiron complex is catalysed by a range of quaternary ammonium salts and an analogous hydrido-manganese complex is obtained from dimanganese decacarbonyl under similar conditions [8], Virtually no reduction occurs in the absence of the quaternary ammonium salt, and the reduction is also suppressed by the presence of carbon monoxide [9], In contrast, dicobalt octacarbonyl reacts with quaternary ammonium fluorides to form complexes which do not reduce nitroarenes. 

Reduction The asymmetric reduction of a series of aryl alkyl ketones with quaternary ammonium fluorides and silanes was reported by Drew and Lawrence [55]. In these reactions, the best catalysts (e.g., 6f) were from the qui ni ne/quinidine series in fact, a fluoride salt prepared from cinchonine gave no induction. The use of trimethoxysilane resulted in faster rates but lower enantioselectivites when compared with tris(trimethoxy)silane. It is interesting that, with the... 

In 1978, Wynberg and coworkers reported the first example of a chiral quaternary ammonium fluoride-catalyzed Michael addition of nitromethane to chalcone (Scheme 9.1) [3]. The reaction was performed in toluene at 20 °C with 10mol% of chiral ammonium salt 1 or 3a and excess potassium fluoride (KF, 15 equiv.), yielding the y-nitro ketone with 10-23% enantiomeric excess (ee). The requisite chiral... 

Currently, it is fair to say that asymmetric synthesis using chiral quaternary ammonium fluorides remains an underdeveloped field, and the various useful stereoselective carbon-carbon bond-forming processes described in this chapter are only the start of an exploration of the vast synthetic potential of this process, particularly when combined with current knowledge of organosilicon chemistry. It seems that the key issue to be addressed is the rational molecular design of chiral quaternary ammonium cations with appropriate steric and electronic properties. These are expected to be readily tunable to impart not only a sufficient reactivity but also an ideal chiral environment to the requisite nucleophile involved in a desired chemical transformation. Clearly, the continuous accumulation of information related to the structure of fluoride salts and their reactivity and selectivity should create a solid basis for this field, offering - in time - a unique yet reliable tool for sophisticated bond construction events with rigorous stereocontrol, under mild conditions. 

The most active catalysts for halogenation with perhalomethane are, evidently, quaternary ammonium fluoride salts. One mol% of tetra- -butylammonium fluoride trihydrate (TBAF) can quantitatively transform a malonate ester to an a-chloro derivative at 25 °C with a half-lifetime of 10 minutes (equation 77)628,629 ... 

At this time, there is relatively little information on alkylation by the solid-liquid phase transfer method, although this approach has been valuable in a variety of other nucleophilic reactions. Most of the mass of alkylation data which has been accumulated involves an organic phase in contact with 50% aqueous sodium hydroxide solution and a catalytic amount of a quaternary ammonium salt (Makosza s method) [2] or a stoichiometric amount of a quaternary ammonium ion pair (Brand-strom s method) [8]. In addition to these, quaternary ammonium fluorides have been... 

When potassium fluoride is combined with a variety of quaternary ammonium salts its reaction rate is accelerated and the overall yields of a vanety of halogen displacements are improved [57, p 112ff. Variables like catalyst type and moisture content of the alkali metal fluoride need to be optimized. In addition, the maximum yield is a function of two parallel reactions direct fluorination and catalyst decomposition due to its low thermal stability in the presence of fluoride ion [5,8, 59, 60] One example is trimethylsilyl fluoride, which can be prepared from the chloride by using either 18-crown-6 (Procedure 3, p 192) or Aliquot 336 in wet chlorobenzene, as illustrated in equation 35 [61],... 

The quaternary ammonium salt 48 derived from (+)-ephedrine was utilized for the enantioselective addition of diethyl zinc to aldehydes.1421 The chiral ammonium fluorides 7 (R=4-CF3 or 2,4-(CF3)2, X=F) were also useful for the enantioselective trifluoro-methylation of aldehydes and ketones with moderate enantioselectivity,1431 shown in Scheme 17... 

The synthesis of polyhalide salts, R4NX , used in electrophilic substitution reactions, are described in Chapter 2 and H-bonded complexed salts with the free acid, R4NHX2, which are used for example in acid-catalysed cleavage reactions and in electrophilic addition reactions with alkenes, are often produced in situ [33], although the fluorides are obtained by modification of method I.I.I.B. [19, 34], The in situ formation of such salts can inhibit normal nucleophilic reactions [35, 36]. Quaternary ammonium chlorometallates have been synthesized from quaternary ammonium chlorides and transition metal chlorides, such as IrClj and PtCl4, and are highly efficient catalysts for phase-transfer reactions and for metal complex promoted reactions [37]. 

The conversion of acyl chlorides, sulphonyl chlorides and phosphoryl chlorides into the corresponding fluorides using potassium fluoride in the presence of a quaternary ammonium salt has been recorded [44-47]. Optimum yields are obtained when the dry potassium fluoride contains ca. 1% water. 

Aldol and Related Condensations As an elegant extension of the PTC-alkylation reaction, quaternary ammonium catalysts have been efficiently utilized in asymmetric aldol (Scheme 11.17a)" and nitroaldol reactions (Scheme ll.lTb) for the constmction of optically active p-hydroxy-a-amino acids. In most cases, Mukaiyama-aldol-type reactions were performed, in which the coupling of sUyl enol ethers with aldehydes was catalyzed by chiral ammonium fluoride salts, thus avoiding the need of additional bases, and allowing the reaction to be performed under homogeneous conditions. " It is important to note that salts derived from cinchona alkaloids provided preferentially iyw-diastereomers, while Maruoka s catalysts afforded awh-diastereomers. 

Ring nitrogens in pyrazines and the benzo derivatives react with electrophiles to form quaternary ammonium species such as iV-alkylpyrazinium salts and pyrazine iV-oxides. N-Alkylation has generally been performed by treatment with a reactive alkyl iodide. The N-1 nitrogen in 2(l//)-pyrazinone 5 is methylated using chloro(chloromethyl)dimethyl-silane followed by desilylation with cesium fluoride to yield l-methyl-2(l//)-pyrazinone <2000TL4933>. 

The hydrothermal method has been employed in recent years to synthesize a variety of solids that include aluminium phosphates (ALPOs) and other microporous transition-metal phosphates and transition-metal polychalcogenides (Davis Lobo, 1992 Haushalter Mundi, 1992 Liao Kanatzidis, 1990, 1992). Unlike zeolites, synthesis of ALPOs requires acidic or mildly basic conditions and no alkali metal cations. A typical synthetic mixture for making ALPO consists of alumina, H3PO4, water and an organic material such as a quaternary ammonium salt or an amine. The hydrothermal reaction occurs around 373-573 K. The use of fluoride ions, instead of hydroxide ions as mineralizer, allows synthesis of novel microporous materials under acidic conditions (Estermann et al, 1991 Ferey et ai, 1994). 

Renewed interest in the fluorination of quaternary ammonium salts is prompted by the need for rapid fluorination techniques to incorporate 18F (t /f 110 mm) in positron emission tomography (PET) studies One promising approach is displacement of trimethylammomum ion, bound directly to an aromatic ring, by fluoride ion This technique was initially developed with substituted phenyltnmeth-ylammomum perchlorates and unlabeled cesium fluoride in dimethyl sulfoxide or acetonitrile [73] (equation 14)... 

Both experimental and theoretical studies have been reported of fluoro-denitration and fluoro-dechlorination reactions using anhydrous tetrabutylammonium fluoride in DMSO. The absences of ion pairing and strong solvation are critical in contributing to the reactivity of the fluorinating agent24 Quaternary ammonium salts derived from cinchona alkaloids have been shown to be effective catalysts in an improved asymmetric substitution reaction of /1-dicarbonyl compounds with activated fluoroarenes. The products may be functionalized to yield spiro-oxindoles.25... 

It is claimed that addition of catalytic quantities of a quaternary ammonium salt greatly enhances both reactivity and yield [48] in the formation and subsequent reactions of (58). Tertiary fluorinated carbanions, generated from corresponding unsaturated precursors, react with a variety of electrophiles [46, 49,50] (Scheme 25), the most surprising being with fluorocarbon iodides, to give remarkable fluoride-bridged products, e. g. (60) [47],... 

Aldol reactions using a quaternary chinchona alkaloid-based ammonium salt as orga-nocatalyst Several quaternary ammonium salts derived from cinchona alkaloids have proven to be excellent organocatalysts for asymmetric nucleophilic substitutions, Michael reactions and other syntheses. As described in more detail in, e.g., Chapters 3 and 4, those salts act as chiral phase-transfer catalysts. It is, therefore, not surprising that catalysts of type 31 have been also applied in the asymmetric aldol reaction [65, 66], The aldol reactions were performed with the aromatic enolate 30a and benzaldehyde in the presence of ammonium fluoride salts derived from cinchonidine and cinchonine, respectively, as a phase-transfer catalyst (10 mol%). For example, in the presence of the cinchonine-derived catalyst 31 the desired product (S)-32a was formed in 65% yield (Scheme 6.16). The enantioselectivity, however, was low (39% ee) [65],... 

Fluoride ion-assisted desilylation has been extensively used to create an ylid from a /V-silyl methyl-quaternary ammonium salt. Its evolution to final produces) is variable and Sommelet-Hauser and Stevens rearrangement products were obtained (often as major products) in a ratio that can be shifted from one structure to another very close one, as in examples 1 and 2 dealing with //-benzyl salts.246,366 Differences in the solvents used are not significant because in the first example, HMPA does not reverse the ratio, yields and selectivity being just a bit lower, /so-toluene was proposed as an intermediate in example 1 it might also be the intermediate in example 2. Thus product partition reflects the relative ability of the C-H or the C-C bonds to be cleaved to produce aromatization with proton or a-amine carbocation migration. 

The asymmetric organocatalytic transformation of a ketone into an alcohol may be realized with the combination achiral silanexhiral phase-transfer catalyst, such a quaternary ammonium salt. The final alcohol is then recovered by an additional hydrolytic step. The asymmetric reduction of aryl alkyl ketones with silanes has been reported (ee-values up to 70%), the catalysts utilized being ammonium fluorides prepared from the quinine/quinidine series (e.g., 18 in Scheme 11.6) [19]. (For experimental details see Chapter 14.21.1). The more appropriated silanes were (Me3SiO)3SiH or (MeO)3SiH (some examples are... 

For less activated aromatic systems (those without a nitro substituent), the halogcn-ex-changc reaction has been investigated with potassium fluoride in a variety of polar aprotic solvents in the presence or absence of a catalyst (see Table 13). Many different types of catalysts have been investigated these include crown ethers, quaternary ammonium salts, 3,164 pjjos-phonium salts, aminophosphonium salts, compounds containing a phosphorus and an amino function, and inorganic fluorides of boron, aluminum, tin, phosphorus, titanium and zirconium. Different forms of potassium fluoride have been used these include spray-dried potassium fluoride, freeze-dried potassium fluoride, potassium fluoride recryslal-lized from methanol, and potassium fluoride dispersed on caleium fluoride. ... 

TBAF (tetra-w butylammonium fluoride) is a quaternary ammonium salt which serves as a fluoride ion source and is a common reagent for cleaving silyl protecting groups. 

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