Effect of metal nitrate on mechanochemical nitration of toluene

Literature Information

Publication Date 2021-09-13
DOI 10.1039/D1RE00307K
Impact Factor 4.239
Authors

Ashvin Vasudevan, Mirko Schoenitz, Edward L. Dreizin


View Original

Abstract

Mechanochemical nitration of toluene was explored using a planetary mill and MoO3 as catalyst. Different inorganic nitrate salts were used as the nitronium source. Nitration was carried out by initially milling the nitrate salt and the catalyst, and then adding toluene. The amount of nitrate salt used was systematically varied, while the amounts of both the catalyst and toluene were held constant. For most nitrates the greatest yield of mononitrotoluene was observed for conditions where the molar reactant ratio of NO3− to toluene was near 4. Lower yields were observed with either less or more of the nitrate, consistent with limitation by the reactant on one hand, and obscuration of suitable catalytic sites on the other. The observed ratios of para- to ortho-mononitrotoluene were above one, consistently with a mechanism involving nitronium ions positioned at the catalyst surface reacting with toluene directly. Different nitrates resulted in varying mononitrotoluene yields, with copper nitrate showing the highest, and potassium nitrate the lowest yield, respectively. The observed yields were found to correlate with the enthalpy of the bulk reaction forming mononitrotoluene and the hydroxide of the cation of the respective nitrate used.

Related Literature

Functionalization of diazotetronic acid and application in a stereoselective modular synthesis of pulvinone, aspulvinones A–E, G, Q and their analogues

Amarender Manchoju, Ritesh A. Annadate, Lise Desquien, Sunil V. Pansare

2018-08-10 Paper

DOI: 10.1039/C8OB01511B

Back cover

Cover

DOI: 10.1039/C8OB90135J

Synthesis of 1,3-dithiol-2-ones as proligands related to molybdopterin

Ben Bradshaw, David Collison, C. David Garner, John A. Joule

2002-11-27 Paper

DOI: 10.1039/B209217D

Aminative Umpolung cyclization for synthesis of chiral exocyclic vicinal diamines

Feng Liu, Guoqing Zhao, Weiqi Cai, Dongfang Xu, Baoguo Zhao

2018-09-26 Paper

DOI: 10.1039/C8OB02000K

Azlactone-based heterobifunctional linkers with orthogonal clickable groups: efficient tools for bioconjugation with complete atom economy

Hien The Ho, Alexandre Bénard, Gwenaël Forcher, Maël Le Bohec, Véronique Montembault, Sagrario Pascual, Laurent Fontaine

2018-09-19 Communication

DOI: 10.1039/C8OB01807C

Refined methods for the synthesis of meso-substituted A3- and trans-A2B-corroles

Daniel T. Gryko, Beata Koszarna

2002-12-09 Paper

DOI: 10.1039/B208950E

An alternative route for the synthesis of hydroxylated pillar[5]arene-based amphiphiles

Talal F. Al-Azemi, Mickey Vinodh, Fatemeh H. Alipour, Abdirahman A. Mohamod

2018-09-26 Paper

DOI: 10.1039/C8OB02074D

Contents list

Front/Back Matter

DOI: 10.1039/C8OB90138D

Dual function of amino acid ionic liquids (Bmim[AA]) on the degradation of the organophosphorus pesticide, Paraoxon®

Javiera I. Morales, Roberto Figueroa, Mabel Rojas, Daniela Millán, Ricardo A. Tapia, Paulina Pavez

2018-09-18 Paper

DOI: 10.1039/C8OB01928B

You might also like

Compound Q&A

What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?

N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...

52818-63-0N-(4-Methoxybenzyl)-...
Compound Q&A

What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?

When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...

1050507-06-6Ethyl 4-(2-chlorophe...
Compound Q&A

What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?

Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...

628-39-7Diethyldiselane
Compound Q&A

What is the market or research trend for oxocopper (CAS: 12053-18-8)?

The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...

12053-18-8oxocopper; oxo-(oxoc...
Compound Q&A

What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?

The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...

1268519-54-55-{[(2-Methyl-2-prop...
Compound Q&A

What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?

2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...

35981-63-62-(1-Pyrrolidinyl)-4...
Compound Q&A

What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?

2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...

91556-75-12-(3-Pyridinyl)-1-az...
Compound Q&A

How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?

(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...

129704-91-2(S)-Alpha-allyl-prol...
Compound Q&A

What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?

3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...

4857-42-53-Methyl-1,2-oxazole...
Compound Q&A

How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?

Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...

1281816-04-3Lys-SMCC-DM1

Source Journal

Reaction Chemistry & Engineering

Reaction Chemistry & Engineering
CiteScore: 0
Self-citation Rate: 8.8%
Articles per Year: 284

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.