Solvent-free γ-valerolactone hydrogenation to 2-methyltetrahydrofuran catalysed by Ru/C: a reaction network analysis

Literature Information

Publication Date 2013-12-12
DOI 10.1039/C3GC41803K
Impact Factor 10.182
Authors

Mohammad G. Al-Shaal, Adam Dzierbinski, Regina Palkovits


View Original

Abstract

2-Methyltetrahydrofuran (2-MTHF) is considered to be an attractive biomass based platform chemical with high potential as a biofuel compound and as a green solvent. 2-MTHF can be synthesised from bio-based levulinic acid (LA) and γ-valerolactone (GVL). Herein the optimum reaction conditions for the hydrogenation of GVL over Ru/C have been studied. A full conversion of GVL has been obtained under solvent free conditions with a maximum yield of 2-MTHF of 43%. The optimized conditions have been employed in a mechanistic study of the synthesis of 2-MTHF. Several side reactions have been investigated to explore the full reaction network of this heterogeneously catalysed system and to elucidate the factors influencing product selectivity. Additionally an efficient solvent-free hydrogenation reaction of LA into 2-MTHF could be achieved delivering 90% conversion of LA with a yield of 2-MTHF of 61% by removing water from the system in a two-step approach.

Related Literature

Measuring and regulating oxygen levels in microphysiological systems: design, material, and sensor considerations

Kristina R. Rivera, Murat A. Yokus, Patrick D. Erb, Vladimir A. Pozdin

2019-04-02 Tutorial Review

DOI: 10.1039/C8AN02201A

In situ study of RSK2 kinase activity in a single living cell by combining single molecule spectroscopy with activity-based probes

Shengrong Yu, Zhixue Du, Chaoqing Dong, Jicun Ren

2019-04-15 Paper

DOI: 10.1039/C9AN00178F

Full-color emissive carbon-dots targeting cell walls of onion for in situ imaging of heavy metal pollution

Zheng Yao, Zhiqiang Lai, Chengchi Chen, Suting Xiao, Peihui Yang

2019-04-27 Paper

DOI: 10.1039/C9AN00418A

Synchrotron macro ATR-FTIR microspectroscopy for high-resolution chemical mapping of single cells

Jitraporn Vongsvivut, David Pérez-Guaita, Bayden R. Wood, Mark J. Tobin

2019-03-05 Paper

DOI: 10.1039/C8AN01543K

A highly specific and ultrasensitive probe for the imaging of inflammation-induced endogenous hypochlorous acid

Wei Hu, Donghua Wang, Zhiqiang Mao, Zhihong Liu

2019-04-11 Paper

DOI: 10.1039/C9AN00390H

A hybridization chain reaction coupled with gold nanoparticles for allergen gene detection in peanut, soybean and sesame DNAs

Dan Yuan, Yongxin Liu, Jilie Kong, Qin Chen

2019-04-30 Paper

DOI: 10.1039/C9AN00394K

Inside back cover

Cover

DOI: 10.1039/C9AN90059D

On-line detection of radioactive and non-radioactive heavy metals in tobacco smoke using portable laser-induced breakdown spectroscopy

Pengfei Zhang, Zhixuan Huang, Yiwen Ma, Yang Li, Naqash Ali, Qifeng Li, Da Chen

2019-04-16 Paper

DOI: 10.1039/C9AN00050J

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

Green Chemistry

Green Chemistry
CiteScore: 16.1
Self-citation Rate: 7.5%
Articles per Year: 944

Green Chemistry provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on, but not limited to, the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998). Green chemistry is the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry is at the frontiers of this continuously-evolving interdisciplinary science and publishes research that attempts to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. Submissions on all aspects of research relating to the endeavour are welcome. The journal publishes original and significant cutting-edge research that is likely to be of wide general appeal. To be published, work must present a significant advance in green chemistry. Papers must contain a comparison with existing methods and demonstrate advantages over those methods before publication can be considered. For more information please see this Editorial. Coverage includes the following, but is not limited to: Design (e.g. biomimicry, design for degradation/recycling/reduced toxicity…) Reagents & Feedstocks (e.g. renewables, CO2, solvents, auxiliary agents, waste utilization…) Synthesis (e.g. organic, inorganic, synthetic biology…) Catalysis (e.g. homogeneous, heterogeneous, enzyme, whole cell…) Process (e.g. process design, intensification, separations, recycling, efficiency…) Energy (e.g. renewable energy, fuels, photovoltaics, fuel cells, energy storage, energy carriers…) Applications (e.g. electronics, dyes, consumer products, coatings, pharmaceuticals, preservatives, building materials, chemicals for industry/agriculture/mining…) Impact (e.g. safety, metrics, LCA, sustainability, (eco)toxicology…) Green chemistry is, by definition, a continuously-evolving frontier. Therefore, the inclusion of a particular material or technology does not, of itself, guarantee that a paper is suitable for the journal. To be suitable, the novel advance should have the potential for reduced environmental impact relative to the state of the art. Green Chemistry does not normally deal with research associated with 'end-of-pipe' or remediation issues.

Recommended Compounds

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.