98-95-3 Usage
Uses
Used in Chemical Synthesis Industry:
Nitrobenzene is used as a key intermediate in the production of aniline, which is an important industrial precursor. Aniline is primarily used in the manufacture of polyurethanes. Nitrobenzene is also used in the synthesis of other organic compounds, such as acetaminophen (Tylenol), a common over-the-counter analgesic.
Used in Petroleum Refining Industry:
Nitrobenzene is used as a solvent in petroleum refining and in the manufacture of cellulose ethers and acetate. It is also used in Friedel-Crafts reactions to hold the catalyst in solution.
Used in Manufacturing Industry:
Nitrobenzene is used in the production of various products such as benzidine, quinoline, azobenzene, pyroxylin compounds, isocyanates, pesticides, rubber chemicals, pharmaceuticals, and dyes like nigrosines and magenta.
Used in Soap and Perfumery Industry:
Nitrobenzene is used as a flavoring agent and a perfume for soaps.
Used in Shoe and Metal Polishes:
Nitrobenzene is used as an ingredient in metal polishes and shoe polishes.
Used in Environmental Analysis:
Nitrobenzene is used as a standard for detection and analysis, as well as for studying its removal from the environment. Its cytotoxic effects have been studied in a hepatocarcinoma cell line.
Used in Laboratory Applications:
Nitrobenzene can sometimes be used as a solvent, especially for electrophilic reagents in the laboratory.
Special Application:
Nitrobenzene has a special application in masking unpleasant odors emitted from shoe, floor polisher, leather, and paint solvents.
References
https://pubchem.ncbi.nlm.nih.gov/compound/nitrobenzene#section=Top
https://en.wikipedia.org/wiki/Nitrobenzene
Production Methods
Nitrobenzene is produced by the direct nitration of benzene with a mixture of
sulfuric and nitric acids. U.S. capacity for nitrobenzene production is approximately
1.5 billion pounds . The most important use for
nitrobenzene is in the production of aniline. Nearly 98% of the nitrobenzene
produced in the U.S. is converted to aniline.
Preparation
Nitrobenzene is produced commercially by the exothermic nitration of benzene with fuming nitric acid in the presence of a sulfuric acid catalyst at 50 to 65℃. The crude nitrobenzene is passed through washer-separators to remove residual acid and is then distilled to remove benzene and water.
Synthesis Reference(s)
Journal of the American Chemical Society, 95, p. 5198, 1973 DOI: 10.1021/ja00797a017Tetrahedron Letters, 27, p. 2335, 1986 DOI: 10.1016/S0040-4039(00)84522-0
Reactivity Profile
Aluminum chloride added to Nitrobenzene containing about 5% phenol caused a violent explosion [Chem. Eng. News 31:4915. 1953]. Heating a mixture of Nitrobenzene, flake sodium hydroxide and a little water led to an explosion, discussed in [Bretherick's 5th ed. 1995]. Mixed with oxidants, i.e. dinitrogen tetraoxide, fluorodinitromethane, nitric acid, peroxodisulfuric acid, sodium chlorate, tetranitromethane, uranium perchlorate, etc., forms highly sensitive explosive, [Bretherick 5th ed, 1995]. Heated mixtures of Nitrobenzene and tin(IV) chloride produce exothermic decomposition with gas production [Bretherick, 5th Ed., 1995].
Hazard
Toxic by ingestion, inhalation, and skin
absorption. Methemoglobinemia. Possible carcinogen.
Health Hazard
The routes of entry of nitrobenzene intothe body are the inhalation of its vaporsor absorption of the liquid or the vaporthrough the skin and, to a much lesserextent, ingestion. The target organs are theblood, liver, kidneys, and cardiovascular system. Piotrowski (1967) estimated that in anexposure period of 6 hours to a concentration of 5 mg/m3, 18 mg of nitrobenzene wasabsorbed through the lungs and 7 mg throughthe skin in humans. Furthermore, about 80%of inhaled vapor is retained in the respiratorytract. The dermal absorption rate at this concentration level is reported as 1 mg/h, whilethe subcutaneous absorption of the liquidis between 0.2 and 0.3 mg/cm3/h (ACGIH1986).The symptoms of acute toxicity are headache, dizziness, nausea, vomiting, and dyspnea. Subacute and chronic exposure cancause anemia. Nitrobenzene effects the conversion of hemoglobin to methemoglobin. Itis metabolized to aminophenols and nitrophenols to about 30%, which are excreted.
Fire Hazard
Moderate explosion hazard when exposed to heat or flame. Reacts violently with nitric acid, aluminum trichloride plus phenol, aniline plus glycerine, silver perchlorate and nitrogen tetroxide. Avoid aluminum trichloride; aniline; gycerol; sulfuric acid; oxidants; phosphorus pentachloride; potassium; potassium hydroxide. Avoid sunlight, physical damage to container, freezing, and intense heat.
Safety Profile
Confirmed carcinogen.
Human poison by an unspecified route.
Poison experimentally by subcutaneous and
intravenous routes. Moderately toxic by
ingestion, skin contact, and intraperitoneal
routes. Human systemic effects by ingestion:
general anesthetic, respiratory stimulation,
and vascular changes. An experimental
teratogen. Experimental reproductive
effects. Mutation data reported. An eye and
skin irritant. Can cause cyanosis due to
formation of methemoglobin. It is absorbed
rapidly through the skin. The vapors are
hazardous.
to heat and flame. Moderate explosion
hazard when exposed to heat or flame.
Explosive reaction with solid or
concentrated alkali + heat (e.g., sodium
hydroxide or potassium hydroxide),
aluminum chloride + phenol (at 12O°C),
aniline + glycerol + sulfuric acid, nitric +
sulfuric acid + heat. Forms explosive
mixtures with aluminum chloride, oxidants
(e.g., fluorodinitromethane, uranium
perchlorate, tetranitromethane, sodium
chlorate, nitric acid, nitric acid + water,
peroxodsulfuric acid, dinitrogen
tetraoxide), phosphorus pentachloride,
potassium, sulfuric acid. Reacts violently
with aniline + glycerin, N20, AgCLO4. To
fight fne, use water, foam, CO2, dry
chemical. Incompatible with potassium
hydroxide. When heated to decomposition it
emits toxic fumes of NOx. See also NITRO
COMPOUNDS OF AROMATIC
HYDROCARBONS.
Potential Exposure
Nitrobenzene is used in the manufacture
of explosives and aniline dyes and as solvent and intermediate.
It is also used in floor polishes; leather dressings
and polished; and paint solvents, and to mask other
unpleasant odors. Substitution reactions with nitrobenzene
are used to form m-derivatives. Pregnant women may be
especially at risk with respect to nitrobenzene as with many
other chemical compounds, due to transplacental passage
of the agent. Individuals with glucose-6-phosphate dehydrogenase
deficiency may also be special risk groups.
Additionally, because alcohol ingestion or chronic alcoholism
can lower the lethal or toxic dose of nitrobenzene,
individuals consuming alcoholic beverages may be at risk.
Carcinogenicity
Nitrobenzene is reasonably anticipated to be a human carcinogenbased on sufficient evidence of carcinogenicity from studies in experimental animals.
Environmental fate
Biological. In activated sludge, 0.4% of the applied nitrobenzene mineralized to carbon dioxide
after 5 d (Freitag et al., 1985). Under anaerobic conditions using a sewage inoculum, nitrobenzene
degraded to aniline (Hallas and Alexander, 1983). When nitrobenzene (5 and 10 mg/L) was
statically incubated in the dark at 25 °C with yeast extract and settled domestic wastewater
inoculum, complete biodegradation with rapid acclimation was observed after 7 to 14 d (Tabak et
al., 1981). In activated sludge inoculum, 98.0% COD removal was achieved in 5 d. The average
rate of biodegradation was 14.0 mg COD/g?h (Pitter, 1976).
Razo-Flores et al. (1999) studied the fate of nitrobenzene (50 mg/L) in an upward-flow
anaerobic sludge bed reactor containing a mixture of volatile fatty acids and/or glucose as electron
donors. The nitrobenzene loading rate and hydraulic retention time for this experiment were 43
mg/L?d and 28 h, respectively. Nitrobenzene was effectively reduced (>99.9%) to aniline (92%
molar yield) in stoichiometric amounts for the 100-d experiment.
Photolytic. Irradiation of nitrobenzene in the vapor phase produced nitrosobenzene and 4-
nitrophenol (HSDB, 1989). Titanium dioxide suspended in an aqueous solution and irradiated with
UV light (λ = 365 nm) converted nitrobenzene to carbon dioxide at a significant rate (Matthews,
1986). A carbon dioxide yield of 6.7% was achieved when nitrobenzene adsorbed on silica gel
was irradiated with light (λ >290 nm) for 17 h (Freitag et al., 1985). Chemical/Physical. In an aqueous solution, nitrobenzene (100 μM) reacted with Fenton’s
reagent (35 μM). After 15 min, 2-, 3-, and 4-nitrophenol were identified as products. After 6 h,
about 50% of the nitrobenzene was destroyed. The pH of the solution decreased due to the
formation of nitric acid (Lipczynska-Kochany, 1991). Augusti et al. (1998) conducted kinetic
studies for the reaction of nitrobenzene (0.2 mM) and other monocyclic aromatics with Fenton’s
reagent (8 mM hydrogen peroxide; [Fe+2] = 0.1 mM) at 25 °C. They reported a reaction rate
constant of 0.0260/min.
Metabolism
Nitrobenzene vapor is readily absorbed through the skin and lungs. At an airborne
nitrobenzene concentration of 10 mg/m3 humans may absorb 18 to 25 mg in 6 h
through the lungs and from 8 to 19 mg
through the skin in the same length of time
.
Urine is the major route of excretion of nitrobenzene metabolites in rabbits
, rats
and mice . The most abundant metabolite in earlier studies in
rabbits and rats was p-aminophenol. This compound, or its glucuronide or sulfate
conjugates, accounted for 19% to 31% of the
dose. In a later study in rats in which the acid hydrolysis step employed by earlier
workers to cleave conjugates was replaced by enzyme hydrolysis, no p-aminophenol
was found in the urine of male Fischer-344 or CD rats .
About 9% of a nitrobenzene dose was excreted by B6C3F1 mice as the sulfate
conjugate. The major metabolites found in Fischer-344 rat urine were p-hydroxyacetanilide
sulfate (19% of the dose), p-nitrophenol sulfate (20% of the dose) and
m-nitrophenol sulfate (10% of the dose) .
In addition, an unidentified metabolite accounted for about 10% of the dose
.
Male CD rats excreted the same metabolites after an oral dose of nitrobenzene,
but in slightly different proportions. They excreted about half
as much of the dose as the glucuronide or sulfate conjugates of P-hydroxyacetanilide
(9% of the dose) and P-nitrophenol (13% of the dose), approximately the
same amount of m-nitrophenol (8% of the dose), and about twice as much as the
unidentified metabolite. Interestingly, whereas Fischer-344 rats excreted the phenolic
metabolites of nitrobenzene exclusively as sulfates, CD rats excreted the
same metabolites in the free form (15-17% of the total metabolite) and as
glucuronides (4-20% of the total metabolite).
Approximately 4% of the dose also was excreted as p-hydroxyacetanilide by
B6C3F1 mice and as p- and m-nitrophenol (7% and 6% of the dose, respectively)
sulfates, glucuronides and free metabolites .
Clearly, ring hydroxylation and reduction are important metabolic steps in the
biotransformation of nitrobenzene in rabbits, rats, mice and humans .
Since no significant isotope effect was found in the metabolism of deuterated
nitrobenzene to these products in rats in vivo , the o- and
p-nitrophenols may be formed through an arene oxide intermediate. A significant isotope effect was noted in the formation of m-nitrophenol from deuterated
nitrobenzene in the same rats, leading to the conclusion that m-nitrophenol is
formed by a direct oxygen insertion mechanism or by some other mechanism
which does not involve an arene oxide intermediate. The reduction of nitrobenzene
in vivo is largely, if not exclusively, due to the action of anaerobic intestinal
microflora. Treatment with antibiotics totally eliminated the ability of cecal
contents of Fischer-344 rats to reduce nitrobenzene in vitro, and rats treated with
antibiotics eliminated p-hydroxyacetanilide as 0.9% of an oral dose of nitro-benzene. Normal rats excreted 16.2% of an oral dose of nitrobenzene as that
metabolite .
The reduction of most nitro compounds by hepatic microsomes is not detectable
under aerobic conditions, but is readily observable under anaerobic conditions.
Mason and Holtzman proposed that the first intermediate in the microsomal
reduction of nitroaromatic compounds is the nitro anion radical, the product
of a one electron transfer to nitrobenzene or other nitroaromatic compound.
Oxygen would rapidly oxidize the radical to yield the parent nitro compound and
Superoxide anion. Both the nitro anion radical and Superoxide anion are potentially
toxic compounds.
Both P-nitrophenol and P-aminophenol have been detected in human urine after
exposure to nitrobenzene. p-Aminophenol has been found only after large accidental
exposures and acid hydrolysis of
urine. Since acid conditions convert p-acetamidophenol to P-aminophenol, the identity of the metabolite actually excreted is in doubt. P-Nitrophenol
has been found in the urine of volunteers exposed to low inhalation doses of
nitrobenzene, and Kuzelova and Popler have suggested that urinary P-nitrophenol
be used to monitor exposure to nitrobenzene.
Shipping
UN1662 Nitrobenzene, Hazard Class: 6.1;
Labels: 6.1-Poisonous materials.
Purification Methods
Common impurities include nitrotoluene, dinitrothiophene, dinitrobenzene and aniline. Most impurities can be removed by steam distillation in the presence of dilute H2SO4, followed by drying with CaCl2, and shaking with, then distilling at low pressure from BaO, P2O5, AlCl3 or activated alumina. It can also be purified by fractional crystallisation from absolute EtOH (by refrigeration). Another purification process includes extraction with aqueous 2M NaOH, then water, dilute HCl, and water, followed by drying (CaCl2, MgSO4 or CaSO4) and fractional distillation under reduced pressure. The pure material is stored in a brown bottle, in contact with silica gel or CaH2. It is very hygroscopic. [Beilstein 5 H 233, 5 I 124, 5 II 171, 5 III 591, 5 IV 708.]
Toxicity evaluation
The intermediates and products of nitrobenzene reduction
can cause methemoglobinemia (a condition in which the
blood’s ability to carry oxygen is reduced) by accelerating the
oxidation of hemoglobin to methemoglobin. Three primary
metabolic mechanisms have been identified: reduction of
nitrobenzene to aniline by intestinal microflora, its reduction
to aniline occurring in hepatic microsomes and erythrocytes,
and nitrobenzene oxidative metabolism to the nitrophenols
by hepatic microsomes. Many of the toxicological effects are
likely triggered by metabolites of nitrobenzene. For example,
methemoglobinemia is caused by the interaction of hemoglobin
with the products of nitrobenzene reduction (i.e.,
nitrosobenzene, phenylhydroxylamine, and aniline). The
anaerobic metabolism occurring in the gastrointestinal track is
much faster than reduction by the hepatic microsomal fraction;
therefore, the action of bacteria normally present in the
small intestine is an important element in the formation of
methemoglobin.
Incompatibilities
Concentrated nitric acid, nitrogen tetroxide;
caustics; phosphorus pentachloride; chemically-active
metals, such as tin or zinc. Violent reaction with strong oxidizers
and reducing agents. Attacks many plastics. Forms
thermally unstable compounds with many organic and inorganic
compounds.
Waste Disposal
Incineration (982℃, 2.0 seconds
minimum) with scrubbing for nitrogen oxides abatement
. Consult with environmental regulatory agencies
for guidance on acceptable disposal practices. Generators
of waste containing this contaminant (≥100 kg/mo) must
conform with EPA regulations governing storage, transportation,
treatment, and waste disposal.
Check Digit Verification of cas no
The CAS Registry Mumber 98-95-3 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 98-95:
(4*9)+(3*8)+(2*9)+(1*5)=83
83 % 10 = 3
So 98-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H5NO2/c8-7(9)6-4-2-1-3-5-6/h1-5H
98-95-3Relevant articles and documents
Mechanistic Study of Photoelectrochemical Reactions: Phototransient Experiments
Compton, Richard G.,Dryfe, Robert A. W.,Hirst, Judy
, p. 10497 - 10503 (1994)
A novel channel electrode phototransient expriment for the mechanistic study of photoelectrochemical reactions is described in which the evolution of the photocurrent in time is monitored after the stepwise application of light to the system once steady-state transport-limited currents have been established in the dark.It is shown that the phototransient data in combination with steady-state photocurrent/flow rate data can accomplish mechanistic discriminations which may be impossible using the latter data alone.The theory of the experiment is given and a working surface presented which allows the analysis of experimental transients regardless of the cell geometry or solution flow rate used in their measurement.The approach is applied to the photoelectrochemical reduction of p-bromonitrobenzene in acetonitrile solution at a platinum electrode.The process, in the presence of light of wavelengths near 330 nm, is shown to be of the photo-ECE type.
Kinetic Electron Spin Resonance Investigation of the Monohydronitro Free Radical of 2,3,5,6-Tetrachloronitrobenzene
Sutcliffe, Leslie H.
, p. 1467 - 1470 (1985)
The e.s.r. spectrum of the short-lived monohydronitro radical from 2,3,5,6-tetrachloronitrobenzene has been obtained by ultraviolet photolysis.The kinetics and energetics of radical recombination have been measured with the aid of two techniques: (i) switching off the radiation from a 1 kW ultraviolet lamp and (ii) pulses from an ultraviolet laser.The two sets of data are in good agreement.
Homogeneous and Electrochemical Electron-Transfer Reaction of Nitrobenzene Anion Radical Dissolved in Nitrobenzene
Suga, Kosaku,Aoyagui, Shigeru
, p. 2713 - 2718 (1987)
Nitrobenzene anion radical was stably prepared by the electrolytic reduction of nitrobenzene solution containing various kinds and amounts of tetraalkylammonium perchlorates.The rate constants of homogeneous electron-transfer reactions of these nitrobenzene anion radicals with nitrobenzene molecules as a solvent were determined by ESR method at various temperatures.These rate constants at 25 deg C were about 107 dm3 mol-1 s-1 and comparable with the rate constant of electron-transfer reaction between nitrobenzene and its anion radical in N,N-dimethylformamide.The quasi-first order rate constants evaluated from these rate constants were about 108 s-1 and were larger than the rate constants of the intramolecular electron-transfer reactions of the anion radical of bis(p-nitrophenyl) compounds except for bis(p-nitrophenyl)methane.The absorption spectrum of the solution of nitrobenzene anion radical in nitrobenzene containing 0.1 M tetrabutylammonium perchlorate or 0.1 M tetraethylammonium perchlorate showed an additional weak peak at about 800 or 900 nm as well as the ordinary peak.The light energies of these additional peaks were in good agreement with the energy values of the optical electron-transfer reactions evaluated according to the theory of Hush from the activation energies of corresponding thermal electron-transfer reactions.The rate constants of electrochemical electron-transfer reactions and the diffusion coefficients of nitrobenzene anion radical in nitrobenzene were also measured.
Self-powered continuous nitration method and device
-
Paragraph 0069-0072, (2021/07/17)
The invention belongs to the technical field of organic synthesis application, and particularly relates to a self-powered continuous nitration method and device. According to the method, a raw material (or a raw material solution) and mixed acid (or nitric acid) are added into a self-powered continuous reactor at the same time, reaction feed liquid continuously and circularly flows, is mixed and reacts in a tube pass through self-propelling force generated by stirring of an impeller, the mass and heat transfer process is completed, and the target requirement is met. According to the invention, the mass transfer and heat transfer efficiency can be improved, the heat exchange and heat transfer capabilities are improved, the reaction time is shortened, the risk degree of art is reduced, the thermal runaway risk is avoided, the reaction safety is improved, and the realization of chemical industry intrinsic safety large scale production is facilitated.
Liquid phase nitration of benzene catalyzed by a novel salt of molybdovanadophosphoric heteropolyacid
Liu, Jianan,Wang, Yanan,Gong, Shuwen,Duan, Wenzeng,Huang, Xianqiang
, p. 1270 - 1276 (2021/05/19)
A highly efficient and reusable catalyst QA-HPMV was successfully prepared by the reaction of quinoline-2-formic acid (QA) with molybdovanadophosphoric heteropolyacid (H4PMo11VO40, HPMV) for the nitration of benzene. The physical and chemical properties o
A photoresponsive palladium complex of an azopyridyl-triazole ligand: light-controlled solubility drives catalytic activity in the Suzuki coupling reaction
Gazdag, Tamás,Holczbauer, Tamás,Jablonkai, István,Kalapos, Péter Pál,Kunfi, Attila,London, Gábor,Mayer, Péter J.,Németh, Krisztina
, p. 23419 - 23429 (2021/07/13)
Herein, the design and synthesis of a click-derived Pd-complex merged with a photoswitchable azobenzene unit is presented. While in thetrans-form of the switch the complex showed limited solubility, the photogeneratedcis-form rendered the molecule soluble in polar solvents. This light-controllable solubility was exploited to affect the catalytic activity in the Suzuki coupling reaction. The effect of the substrate and catalyst concentration and light intensity on the proceeding and outcome of the reaction was studied. Dehalogenation of the aryl iodide starting material was found to be a major side reaction; however, its occurrence was dependent on the applied light intensity.
The polyhedral nature of selenium-catalysed reactions: Se(iv) species instead of Se(vi) species make the difference in the on water selenium-mediated oxidation of arylamines
Capperucci, Antonella,Dalia, Camilla,Tanini, Damiano
supporting information, p. 5680 - 5686 (2021/08/16)
Selenium-catalysed oxidations are highly sought after in organic synthesis and biology. Herein, we report our studies on the on water selenium mediated oxidation of anilines. In the presence of diphenyl diselenide or benzeneseleninic acid, anilines react with hydrogen peroxide, providing direct and selective access to nitroarenes. On the other hand, the use of selenium dioxide or sodium selenite leads to azoxyarenes. Careful mechanistic analysis and 77Se NMR studies revealed that only Se(iv) species, such as benzeneperoxyseleninic acid, are the active oxidants involved in the catalytic cycle operating in water and leading to nitroarenes. While other selenium-catalysed oxidations occurring in organic solvents have been recently demonstrated to proceed through Se(vi) key intermediates, the on water oxidation of anilines to nitroarenes does not. These findings shed new light on the multifaceted nature of organoselenium-catalysed transformations and open new directions to exploit selenium-based catalysis.
Alternative method for the synthesis of triazenes from aryl diazonium salts
Abrams
, (2021/05/10)
An alternative mild method for access to 1-aryl-3,3-dimethyl alkyl triazenes is described. This protocol employs the dropwise addition of a methanolic solution of a carboxylate (RCO2M) or carbonate (CO32?) to a gently heated DMF solution containing an aryl diazonium salt (ArN2+), that had been previously isolated. Presumably homolysis of the weak N–O bond of diazo ether adducts formed in this operation initiates radical pathways that lead to the generation of triazene product. DMF serves as not only a one-electron donor to the diazonium salts employed in this process, but also as a source of dimethylamine radicals that act as a nucleophilic coupling partner. The reaction provides modest yields (ca. 20–40%) across an array of aryl diazonium salts that contain various substitution. Furthermore this unique approach to triazenes contrasts with traditional methods that employ dimethyl amine in reagent form which directly couples with diazonium salts. Seemingly, only one other example employing somewhat similar reaction conditions to this current investigation en route to triazenes has been reported, albeit with lower yields and for one representative example furnished as a side-product. The current work here improves upon the efficiency of this reported result, and further expands the reaction scope.
New insight into the electrochemical reduction of different aryldiazonium salts in aqueous solutions
Goljani, Hamed,Nematollahi, Davood,Sepehrmansourie, Hassan,Tavakkoli, Zahra,Zolfigol, Mohammad Ali
, p. 25811 - 25815 (2021/08/09)
Electrochemical reduction of different aryldiazonium salts in aqueous solution was studied in this work and it is shown that the aryldiazonium salts are converted to the corresponding aryl radical and aryl anion. The results of this research indicate that the reduction of aryldiazonium salts takes place in two single-electron steps. Our data show that when the substituted group on the phenyl ring is H, Cl, OH, NO2, OCH3or SO3?, the corresponding diazonium salt shows poor adsorption characteristics, but when the substituted group is methyl, the corresponding diazonium salt shows strong adsorption characteristics. In the latter case, the voltammogram exhibits three cathodic peaks. In addition, the effect of various substitutions on the aryldiazonium reduction was studied by Hammett's method. The data are show that with increasing electron withdrawing capacity of the substituent, the reduction of corresponding diazonium salt becomes easier.
Exploiting a silver-bismuth hybrid material as heterogeneous noble metal catalyst for decarboxylations and decarboxylative deuterations of carboxylic acids under batch and continuous flow conditions
?tv?s, Sándor B.,Fül?p, Ferenc,Kónya, Zoltán,Kukovecz, ákos,Márton, András,Mészáros, Rebeka,Pálinkó, István,Szabados, Márton,Varga, Gábor
, p. 4685 - 4696 (2021/07/12)
Herein, we report novel catalytic methodologies for protodecarboxylations and decarboxylative deuterations of carboxylic acids utilizing a silver-containing hybrid material as a heterogeneous noble metal catalyst. After an initial batch method development, a chemically intensified continuous flow process was established in a simple packed-bed system which enabled gram-scale protodecarboxlyations without detectable structural degradation of the catalyst. The scope and applicability of the batch and flow processes were demonstrated through decarboxylations of a diverse set of aromatic carboxylic acids. Catalytic decarboxylative deuterations were achieved on the basis of the reaction conditions developed for the protodecarboxylations using D2O as a readily available deuterium source.
