17539-79-6

Upstream product

• 96-09-3 styrene oxide 
• 622-58-2 p-Tolylisocyanate 
• 124-38-9 carbon dioxide 
• 106-49-0 p-toluidine 
• 4427-92-3 4-Phenyl-1,3-dioxolan-2-one 
• 100-42-5 styrene 

Downstream Products

• 17539-90-1 N-(p-tolyl)-1-phenyl-2-aminoethanol 

Relevant academic research and scientific papers

Isocyanurate Formation During Oxazolidinone Synthesis from Epoxides and Isocyanates Catalysed by a Chromium(Salphen) Complex

Chromium(salphen) complex 10 is found to be a catalyst for the preparation of oxazolidinones from epoxides and isocyanates. Using the optimal reaction conditions (1.5 mol % of chromium(salphen) complex 10 at 80 °C in toluene for 4 hours), six epoxides wer

The catalytic system ‘Rhodamine B/additive’ for the chemical fixation of CO2

The catalytic system ‘Rhodamine B/additive’ was introduced to promote the CO2 reactions. We synthesized various cyclic carbonates in good to excellent yields under the catalysis of rhodamine B and TBAB. A variety of 2-oxazolidinone derivatives were obtained in the presence of rhodamine B and DBU.

Method for synthesizing five-membered oxygen-containing heterocyclic compound

The invention discloses a method for synthesizing a five-membered oxygen-containing heterocyclic compound, which is characterized in that epoxide and hetero-accumulated diene are used as raw materials, and the five-membered oxygen-containing heterocyclic

Method for catalytically synthesizing oxazolidinone by using imidazolium salt

The invention discloses a method for catalytically synthesizing oxazolidinone by using imidazolium salt, and belongs to the technical field of organic synthesis. According to the invention, epoxide and isocyanate are adopted as raw materials, and the cata

Green synthesis of Dy2Ce2O7 Nanoparticles Immobilized on Fibrous Nano-silica for Synthesis of 3-Aryl-2-oxazolidinones from Alkenes, Amines, and Carbon Dioxide

Abstract: In the present research, a new dendritic fibrous nanosilica (DFNS) based nanocatalyst (DFNS/Dy2Ce2O7) that has high surface zone as well as easy availability of active zones has been properly expanded using an easy approach. DFNS that possess high surface zone is functionalized by amino groups working as the anchors such that the nanoparticles of Dy2Ce2O7 are fine-dispersed onto the DFNS microspheres fibres, without any aggregation. The nanoparticles of Dy2Ce2O7 are produced by a green approach in the attendance of gum of ferula assa-foetida of Dy(NO3)3 and (NH4)2Ce(NO3)6 as ceric and dysprosium sources. The structural evaluation of the samples proved the synthesis of Dy2Ce2O7 NPs. Moreover, a straight way for the production of 3-aryl-2-oxazolidinones by carbon dioxide, olefins, and anilines was obtained utilizing nano catalyst of DFNS/Dy2Ce2O7 in the lack of solvent. The reaction works properly at moderate states. This method that is cheap and simple may be used to different olefins that has proper to excellent 3-aryl-2-oxazolidinones productions. The catalyst may be simply recycled for ten times without considerable losing the activity of its catalytic. Graphic Abstract: [Figure not available: see fulltext.]

Squaramide–Quaternary Ammonium Salt as an Effective Binary Organocatalytic System for Oxazolidinone Synthesis from Isocyanates and Epoxides

Squaramide–quaternary ammonium salt is illustrated as a simple, tunable, and competent metal-free binary catalytic platform for the atom-economic conversion of epoxides and isocyanates into oxazolidinones. Although, various metal catalysts have been employed for the title reaction, application of organocatalysis is scarce. At first, a rational survey of catalytic activity of several air-stable and architecturally distinct squaramides was undertaken. Thereafter, the impact on catalytic capability of different parameters, such as temperature, catalyst loading, and nature of nucleophiles, was examined. This binary organocatalytic system for the oxazolidinone synthesis, composed of a squaramide entity along with a suitable halide anion, was applied to the challenging conversion of a plethora of alkyl- and aryl-substituted epoxides– including disubstituted and enantioenriched ones– and isocyanates into the corresponding oxazolidinones in high-to-excellent yields. The time-dependent formation of oxazolidinone from epoxide and isocyanate was monitored by FTIR-ATR and 1H NMR spectroscopy and the scalability of this process was also described. In light of 1H NMR experiment, a hydrogen-bonding/anion-binding mechanism was proposed wherein the nucleophilic ring-opening operation, and oxo- and carbamate-anions stabilization occur cooperatively towards isocyanate fixation.

Synthesis of N-aryl-2-oxazolidinones from cyclic carbonates and aromatic amines catalyzed by bio-catalyst

A convenient and effective method of synthesizing 3-aryl-2-oxazolidinones from cyclic carbonates and aryl amines catalyzed by bio-catalyst adenine in the presence of Et3N under solvent-free conditions is described. The protocol is suitable for the wide scope of substrates, e.g. cyclic carbonates with or without substitutes, and aryl amines with either electron-withdrawing or electron-donating group. The products were obtained in good to excellent yields under the optimal conditions, even in steric hindered cases. The effect of reaction time, temperature, loading of catalyst, and amount of starting materials in the reaction were investigated, and the reaction mechanism is discussed.

Potassium phosphate-catalyzed one-pot synthesis of 3-aryl-2-oxazolidinones from epoxides, amines, and atmospheric carbon dioxide

Potassium phosphate was found to be a highly active catalyst in the three-component cycloaddition of amines, epoxides, and carbon dioxide in DMF at ambient temperature to form 3-aryl-2-oxazolidinones. Atmospheric CO2 and a broad range of amines were employed in this transformation. Aryl isocyanate and 1,2-aminoalcohol were generated in situ as key intermediates. This one-pot reaction is applicable to a variety of terminal epoxides and amines. The key advantages are high yields, simple work-up, inexpensive catalysts, and a practical ten gram-scale synthesis.

Synthesis of Oxazolidinones from Epoxides and Isocyanates Catalysed by Aluminium Heteroscorpionate Complexes

The combination of an aluminium(heteroscorpionate) complex and tetrabutylammonium bromide acts as a highly efficient catalyst system for the synthesis of oxazolidinones from epoxides and isocyanates. Twenty two complexes were tested derived from a range o

VanadiumV(salen) catalysed synthesis of oxazolidinones from epoxides and isocyanates

The combination of a vanadiumV(salen) complex V +O(salen) EtOSO3- and tetrabutylammonium bromide forms a highly active catalyst system for the reaction between epoxides and isocyanates leading to oxazolidinones.