802294-64-0Relevant articles and documents
ON-LINE GC-IR IDENTIFICATION OF THE PRODUCTS OF HEXADECANE OXIDATION
Imre, L.,Danoczy, E.,Jalsovszky, G.,Holly S.
, p. 35 - 38 (1982)
The GC-IR investigation of the oxidation products of hexadecane indicated that the main components of the reaction mixture are carboxylic acids, ketones and gamma-lactones.The ir spectra of GC-effluents allow primarly the type of compounds to be determine
CO2 as oxidant: an unusual light-assisted catalyst free oxidation of aldehydes to acids under mild conditions
Aniya, Vineet,Jain, Suman L.,Khan, Shafiur Rehman,Khatri, Praveen K.,Kumari, Alka,Naresh, K.,Ray, Anjan,Saini, Sandhya
, p. 2208 - 2211 (2022/02/17)
A novel visible light-driven catalyst-free oxidation of aldehydes using CO2 both in batch and flow photoreactors to get corresponding acids along with the formation of CO in the effluent gas is described.
Cu(II)-Based Ionic Liquid Supported on SBA-15 Nanoparticles Catalyst for the Oxidation of Various Alcohols into Carboxylic Acids in the Presence of CO2
Peng, Qi,Hou, Dejian,Chen, Yanwu,Lin, Litian,Sadeghzadeh, Seyed Mohsen
, p. 1308 - 1320 (2021/07/26)
In this paper, we have produced carboxylic acids by the oxidation of various alcohols in the presence of CO2 using SBA-15/IL supported Cu(II) (SBA-15/IL/Cu(II)) as nanocatalyst. The obtained products showed to have excellent yields by taking into account of SBA-15/IL/Cu(II) nanocatalyst. In addition, the analysis of EDX, SEM, TGA, TEM, XPS, and FT-IR showed the heterogeneous structure of SBA-15/IL/Cu (II) catalyst. It is determined that, after using SBA-15 excess, the catalytic stability of the system was enhanced. Moreover, hot filtration provided a full vision in the heterogeneous catalyst nature. The recycling as well as reuse of the catalyst were studied in cases of coupling reactions many times. Moreover, we have studied the mechanism of the coupling reactions. Graphic Abstract: [Figure not available: see fulltext.]
Transformation of Thioacids into Carboxylic Acids via a Visible-Light-Promoted Atomic Substitution Process
Fu, Qiang,Liang, Fu-Shun,Lou, Da-Wei,Pan, Gao-Feng,Wang, Rui,Wu, Min,Xie, Kai-Jun
supporting information, p. 2020 - 2024 (2022/03/31)
A visible-light-promoted atomic substitution reaction for transforming thiocacids into carboxylic acids with dimethyl sulfoxide (DMSO) as the oxygen source has been developed, affording various alkyl and aryl carboxylic acids in over 90% yields. The atomic substitution process proceeds smoothly through the photochemical reactivity of the formed hydrogen-bonding adduct between thioacids and DMSO. A DMSO-involved proton-coupled electron transfer (PCET) and the simultaneous generation of thiyl and hydroxyl radicals are proposed to be key steps for realizing the transformation.
carba Nicotinamide Adenine Dinucleotide Phosphate: Robust Cofactor for Redox Biocatalysis
D?ring, Manuel,Sieber, Volker,Simon, Robert C.,Tafertshofer, Georg,Zachos, Ioannis
supporting information, p. 14701 - 14706 (2021/05/13)
Here we report a new robust nicotinamide dinucleotide phosphate cofactor analog (carba-NADP+) and its acceptance by many enzymes in the class of oxidoreductases. Replacing one ribose oxygen with a methylene group of the natural NADP+ was found to enhance stability dramatically. Decomposition experiments at moderate and high temperatures with the cofactors showed a drastic increase in half-life time at elevated temperatures since it significantly disfavors hydrolysis of the pyridinium-N?glycoside bond. Overall, more than 27 different oxidoreductases were successfully tested, and a thorough analytical characterization and comparison is given. The cofactor carba-NADP+ opens up the field of redox-biocatalysis under harsh conditions.
PROCESS FOR THE PREPARATION OF C3-5 SATURATED ALIPHATIC CARBOXYLIC ACIDS
-
Page/Page column 19, (2021/07/17)
A process for the preparation of a saturated aliphatic carboxylic acid with 3 to 5 carbon atoms by oxidation of the corresponding aldehyde with oxygen in which (a) the corresponding aldehyde is converted with oxygen at a temperature of 40 to 150°C and an oxygen partial pressure of 0.001 to 1 MPa to obtain a mixture containing the saturated aliphatic carboxylic acid and ≤ 2 mol-% of the corresponding aldehyde with respect to the saturated aliphatic carboxylic acid, (b) the mixture obtained in step (a) is thermally treated in the liquid phase at a temperature of 80 to 250°C and a pressure of 0.1 to 2 MPa abs for 0.25 to 100 hours, and (c) the mixture obtained in step (b) is distilled in a distillation apparatus to obtain a distillate containing ≥ 90 wt.-% of the saturated aliphatic carboxylic acid and having an active oxygen content of 0 to 25 wt.-ppm based on the distillate.
Influence of Solvents on the Oxidation Kinetics of Aldehydic Group Compounds by Diethylammonium Chloro-chromate
Bishnoi, Pramila,Chandora, Divya,Ganpatram,Prakash, Om,Sharma, Vinita
, p. 1329 - 1335 (2022/01/24)
The redox studies of some compounds containing aldehydic functional groups by diethylammonium chloro-chromate (DEACC) in dimethylsulfoxide leading a product forming to acid of correspondimg order. Reactions are found to be in unit order with oxidant while a fractional order (less than unity) was found w. r. t. reductants. The redox reactions are influenced with acid, the acid dependence is governed by this equation: kobs = a + b[H+]. When isomeric form of aldehyde, that is Me-CDO is oxidised with the same oxidant it was observed a considerable K. I.E. (Deuterium effect; kH/kD = 05.69 at 298 K). The reaction of Acetaldehyde was done in various non aqueous medium, soluble or miscible in DMSO. The effect of solvent is studied fitting our data in the solvent model of Taft's and Swain's applied for this purpose. Rate constants are correlating very well with already reported Taft's values of s*; further the reaction constants are negative in nature. Suitable mechanism involving are proposed with transfer of hydride ion.
An efficient and ultrastable single-Rh-site catalyst on a porous organic polymer for heterogeneous hydrocarboxylation of olefins
Yuan, Qiao,Song, Xiangen,Feng, Siquan,Jiang, Miao,Yan, Li,Li, Jingwei,Ding, Yunjie
supporting information, p. 472 - 475 (2021/01/25)
A heterogeneous hydrocarboxylation process of olefins to obtain carboxylic acids with one more carbon was first realized using a single-Rh-site catalyst formed on porous organic polymer (Rh1/POPs). The in situ formation of hydrophilic porous ionic polymer from hydrophobic POPs with the help of CH3I led to high activity and superb stability.
Hydrolysis of amides to carboxylic acids catalyzed by Nb2O5
Siddiki,Rashed, Md. Nurnobi,Touchy, Abeda Sultana,Jamil, Md. A. R.,Jing, Yuan,Toyao, Takashi,Maeno, Zen,Shimizu, Ken-Ichi
, p. 1949 - 1960 (2021/03/26)
Hydrolysis of amides to carboxylic acids is an industrially important reaction but is challenging due to the difficulty of cleaving the resonance stabilized amidic C-N bond. Twenty-three heterogeneous and homogenous catalysts were examined in the hydrolysis of acetamide. Results showed that Nb2O5was the most effective heterogeneous catalyst with the greatest yield of acetic acid. A series of Nb2O5catalysts calcined at various temperatures were characterized and tested in the hydrolysis of acetamide to determine the effects of crystal phase and surface properties of Nb2O5on catalytic performance. The high catalytic performance observed was attributed mainly to the facile activation of the carbonyl bond by Lewis acid sites that function even in the presence of basic inhibitors (NH3and H2O). The catalytic studies showed the synthetic advantages of the present method, such as simple operation, catalyst recyclability, additive free, solvent free, and wide substrate scope (>40 examples; up to 95% isolated yield).
Au-catalyzed electrochemical oxidation of alcohols using an electrochemical column flow cell
Suga, Tatsuya,Shida, Naoki,Atobe, Mahito
, (2021/02/09)
A novel green system for the electrochemical oxidation of alcohols is demonstrated using a column flow cell. Voltammetric analysis revealed that the oxidation of 1-phenylethanol and benzaldehyde are promoted by using both an Au-electrode and an alkaline medium. To conduct such reaction with a column flow cell, we developed a method to modify a carbon-fiber thread with Au nanoparticles. The column carbon-fiber thread electrode modified with Au nanoparticles showed a high surface area, enabling the efficient electrochemical oxidation of various alcohols.
