Benzoylation for the recovery of structure directing agent (di-n-propylamine) from the process effluent of aluminophosphate synthesis
Literature Information
Nageswara N. Rao, Smita Masid
Di-n-propylamine (DPA), a structure directing agent for (silico)aluminophosphate (AlPO4) synthesis, is lost into the mother liquor (ML, 5–6 wt%) from the filtration step. A simple benzoylation reaction could recover DPA as N,N,-dipropylbenzamide (DPBA). The reaction also leads to the recovery of more AlPO4 and a decrease in the pollution caused by the ML.
Recommended Journals

Journal of the Indian Institute of Science

Critical Reviews in Solid State and Materials Sciences

Colloid Journal

Bioorganic & Medicinal Chemistry

Herald of the Russian Academy of Sciences

Electroanalysis

Bioorganic & Medicinal Chemistry Letters

Atomization and Sprays

NDT & E International

Heteroatom Chemistry
Related Literature
Temperature-induced large amplitude conformational change in the complex of oxatub[4]arene revealed via rotaxane synthesis
Dong-Hao Li, Liu-Pan Yang, Hongxin Chai, Fei Jia, Hua Ke, Wei Jiang
DOI: 10.1039/C9QO00159J
Asymmetric hydrogenation of α-hydroxy ketones with an iridium/f-amphox catalyst: efficient access to chiral 1,2-diols
Weilong Wu, Yun Xie, Pan Li, Xiuxiu Li, Yuanhua Liu, Xiu-Qin Dong
DOI: 10.1039/C6QO00810K
Organocatalytic C–C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins
Junyu Xu, Jing Cao, Chao Fang, Tao Lu, Ding Du
DOI: 10.1039/C6QO00734A
Pyrene-fused bisphenazinothiadiazoles with red to NIR electroluminescence
Diego Cortizo-Lacalle, Antonio Pertegás, Manuel Melle-Franco, Henk J. Bolink
DOI: 10.1039/C7QO00227K
Iodine(iii)-induced regioselective carbocyclization of terminal alkynes: a facile approach to prepare 1,1-diiodomethylene substituted cyclic compounds
Zeyu Wang, Jiang Zhong, Chen Zheng, Renhua Fan
DOI: 10.1039/C6QO00822D
Synthesis of quinazolinones via radical cyclization of α-azidyl benzamides
Tonghao Yang, Weixia Wang, Dian Wei, Tianqi Zhang, Bing Han, Wei Yu
DOI: 10.1039/C6QO00656F
Ir-Catalyzed ring-opening of oxa(aza)benzonorbornadienes with water or alcohols
Xin Yang, Wen Yang, Yongqi Yao, Yingying Deng, Dingqiao Yang
DOI: 10.1039/C8QO01403E
Synthesis of 2,3-diaza-anthraquinones via the bidentate Lewis acid catalysed inverse electron-demand Diels–Alder (IEDDA) reaction
Longcheng Hong, Sebastian Ahles, Marcel A. Strauss, Christian Logemann, Hermann A. Wegner
DOI: 10.1039/C7QO00172J
A new water-soluble cavitand with deeper guest binding properties‡
Faiz-Ur Rahman, Yang Yu
DOI: 10.1039/C9QO00049F
Pentadecaphenylenes: synthesis, self-assembly and complexation with fullerene C60
M. Jalilur Rahman, Hideyuki Shimizu, Masashi Hasegawa, Masahiko Iyoda
DOI: 10.1039/C7QO00258K
You might also like
What precautions should be taken when handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3)?
When handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3), safety go...
What is 4-(3,5-Difluorophenyl)aniline (CAS: 405058-00-6)?
4-(3,5-Difluorophenyl)aniline is an aromatic organic compound with the CAS numbe...
How is 5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid (CAS: 338982-07-3) typically synthesized?
5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid can ...
What is the market or research trend for 4-Benzylaniline hydrochloride (CAS: 6317-57-3)?
The market for 4-Benzylaniline hydrochloride (CAS: 6317-57-3) is steadily growin...
Is [3-(Diethylsulfamoyl)phenyl]boronic acid (CAS: 871329-58-7) safe?
[3-(Diethylsulfamoyl)phenyl]boronic acid is generally considered safe when handl...
What are the main uses of 3-Bromo-2,5-dimethoxyaniline (CAS: 115929-62-9)?
3-Bromo-2,5-dimethoxyaniline is mainly used in the pharmaceutical and chemical i...
What regulatory guidelines apply to N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7)?
N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7) is subject to ...
What industries use Carbamic acid, N-[(5S)-5,6-diamino-6-oxohexyl]-, 1,1-dimethylethyl ester (CAS: 24828-96-4)?
This compound is primarily used in the pharmaceutical industry for the synthesis...
How should 2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) be stored?
2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) sho...
What industries use Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9)?
Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9) is utilized in the pharma...
Source Journal
Green Chemistry

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.




![6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-6-carboxylic acid structure 6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-6-carboxylic acid structure](https://static.chemtradehub.com/structs/136/1369160-12-2-6524.webp)