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Journal ArticleDOI

Intensification of rates and selectivity using tri-liquid versus Bi-liquid phase transfer catalysis : Insight into reduction of 4-nitro-o-xylene with sodium sulfide

TLDR
In this paper, the phase transfer catalysis (PTC) reactions are conducted under milder conditions, using less-expensive solvents at much faster reaction rates and improved selectivities to desired products.
Abstract
Reactions in three immiscible liquid phases are attractive, and one of the phases can be the locale of the reaction, which will have a dramatic effect on the product distribution in complex reactions. Thus, converting a bi-liquid (L-L) system into tri-liquid (L-L-L) phases is of considerable scientific and commercial interest. Such systems encounter mass-transfer resistances for transfer across two interfaces and the kinetic analysis becomes difficult. In the case of phase transfer catalysis (PTC), a majority of preparatory and industrial reactions are conducted in two phases. The L-L PTC reactions are conducted under milder conditions, using less-expensive solvents at much faster reaction rates and improved selectivities to desired products. However, the phase transfer catalyst is not recovered but treated as waste, because the quantities are very small and do not contribute much to the expensive product. L-L PTC can be elegantly modified to convert it to L-L-L PTC, to recover and reuse the catalyst and also to enhance selectivity, thereby improving profitability and environmental benefits. 3,4-Dimethyl aniline is a useful starting material for the production of riboflavin (vitamin B2) and also is used as a precursor for many drugs. It can be produced via the reduction of 4-nitro-o-xylene in toluene with aqueous sodium sulfide, using tetrabutylammonium bromide (TBAB) as a catalyst under L-L-L PTC at 80 °C. Comparison between tri- and bi-liquid phases was also conducted, and it was observed that, under L-L-L conditions, the rates of reaction of the formation of 3,4-dimethyl aniline had been dramatically enhanced. The kinetics and mechanism of complex L-L-L PTC processes have been explored in detail. The yield, based on the initial amount of reactant, was >95%, and the selectivity was 100%.

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Citations
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Journal ArticleDOI

Selective oxidation of methyl mandelate to methyl phenyl glyoxylate using liquid–liquid–liquid phase transfer catalysis

TL;DR: In this article, the authors used liquid-liquid-liquid phase transfer catalysis (L-L-PTC) with tetra-butyl ammonium bromide as a catalyst at 45°C.
Journal ArticleDOI

Modeling of microwave irradiated liquid–liquid–liquid (MILLL) phase transfer catalyzed green synthesis of benzyl thiocyanate

TL;DR: In this article, a synergistic combination of low energy microwave irradiated liquid-liquid-liquid (MILLL) PTC reaction has been brought out in intensification of reaction rates and selectivity towards benzylthiocyanate in nucleophilic substitution reaction of benzyl chloride.
Journal ArticleDOI

Tri-liquid system in the synthesis of dialkyl peroxides using tetraalkylammonium salts as phase-transfer catalysts

TL;DR: In this paper, a phase-transfer catalyst is used to form an insoluble third-liquid phase between the organic and aqueous phases that enables the catalyst to be recycled multiple times.
Journal ArticleDOI

Process intensification and waste minimization in liquid–liquid–liquid phase transfer catalyzed selective synthesis of mandelic acid

TL;DR: In this paper, mandelic acid was produced by L-L-L PTC reaction of dichlorocarbene with benzaldehyde in the presence of poly ethylene glycol (PEG) 4000 as the catalyst.
Journal ArticleDOI

Environment Molecules Boost the Chemoselective Hydrogenation of Nitroarenes on Cobalt Single-Atom Catalysts

TL;DR: In this article , the authors report that the environment moieties, such as protic solvents, and external bases, can boost the cobalt SAC-catalyzed chemoselective hydrogenation of nitroarenes.
References
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BookDOI

Handbook of phase transfer catalysis

Yoel Sasson, +1 more
TL;DR: Nucleophilic aliphatic and aromatic substitutions in phase transfer catalysis mechanism and synthetic applications kinetics and mechanism in phase-transfer catalysis synthesis and properties as mentioned in this paper.
Journal ArticleDOI

A general procedure for mild and rapid reduction of aliphatic and aromatic nitro compounds using ammonium formate as a catalytic hydrogen transfer agent

TL;DR: In this paper, various aliphatic and aromatic nitro compounds were selectively and rapidly reduced to their corresponding amino derivatives in very good yield using anhydrous ammonium formate as a catalytic hydrogen transfer agent.
Journal ArticleDOI

Insight into Green Phase Transfer Catalysis

TL;DR: In this article, a new insight into PTC for some reactions of industrial importance is provided, where several steps are combined in a cascade-engineered PTC, if used at all, without separation, or with partial replenishment of the reactants for all the steps to get substantial waste minimization.
Journal ArticleDOI

Kinetics of the n-Butoxylation of p-Chloronitrobenzene under Liquid−Liquid−Liquid Phase Transfer Catalysis

TL;DR: In this paper, the n-butoxylation of p-chloronitrobenzene (PCNB) with nbutyl alcohol and sodium hydroxide under L−L−L PTC, including kinetic modeling.
Journal ArticleDOI

Liquid‐Liquid‐Liquid Phase Transfer Catalysis: A Novel and Green Concept for Selective Reduction of Substituted Nitroaromatics

TL;DR: In this article, a variety of nitroaromatics was reduced by using aqueous sodium sulfide, and tetrabutylammonium bromide (TBAB) as the phase transfer catalyst by choosing appropriate concentrations which resulted in three immiscible liquid phases.
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