696646-58-9

Upstream product

• 50-00-0 formaldehyd 
• 2409-61-2 di(p-tolyl)phosphine oxide 
• 109-73-9 N-butylamine 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 106-38-7 para-bromotoluene 

Relevant academic research and scientific papers

Synthesis and ionophoric properties of α,ω-diphosphorylated aza podands: II. Kabachnik-fields reaction as a method for design of α,ω-diphosphorylated aza podands and their use for determination of metal ions

Methods of the design of podands with α-aminomethylphosphine oxide terminal groups with the purpose of investigation of the ionophoric properties of the podands and their use as components of ion-selective electrodes are analyzed. The most convenient procedure is a one-pot synthesis based on the Kabachnik-Fields reaction in a system comprising a dialkyl(aryl)phosphinous acid, formaldehyde, and a diamine. An alternative procedure is two-stage and involves the reaction of a primary amine with a phosphinous acid and formaldehyde to form an α-aminomethyldialkyl(aryl)phosphine oxide in the first stage and cross-linking of two molecules of this compound via reaction with a dihalooligoether of the corresponding length in the second. Advantages and disadvantages of both procedures are considered. Electrode-active properties of the prepared aza podands are studied to show that ion-selective electrodes on their basis can be used for selective determination of low concentrations of alkali and alkaline-earth metal ions. 2005 Pleiades Publishing, Inc.

Microwave-assisted synthesis of N,N-bis(phosphinoylmethyl)amines and N,N,N-tris(phosphinoylmethyl)amines bearing different substituents on the phosphorus atoms

A family of N,N-bis(phosphinoylmethyl)amines bearing different substituents on the phosphorus atoms was synthesized by the microwave-assisted and catalyst-free Kabachnik–Fields reaction of (aminomethyl)phosphine oxides with paraformaldehyde and diphenylphosphine oxide. The three-component condensation of N,N-bis(phosphinoylmethyl)amine, paraformaldehyde and a secondary phosphine oxide affording N,N,N-tris(phosphinoylmethyl)amine derivatives was also elaborated. This method is a novel approach for the synthesis of the target products.

Microwave-assisted synthesis of α-aminophosphine oxides

Aminophosphine oxides and bis(phosphinoylmethyl)amines were synthesized by the microwave (MW)-assisted Kabachnik-Fields reaction of primary amines, paraformaldehyde and secondary phosphine oxides. The bisphosphines obtained after deoxygenation of the bis(phosphinoymethyl)amine derivatives were utilized in the synthesis of cyclic transition metal complexes.

Synthesis and use of α-aminophosphine oxides and N,N-bis(phosphinoylmethyl)amines - A study on the related ring platinum complexes

The Kabachnik-Fields condensation was extended using secondary phosphine oxides, such as dibenzylphosphine oxide and bis(4-methylphenyl)phosphine oxide as the P-reactant in reaction with formaldehyde and different primary amines. Besides the α-aminophosphine oxides, the corresponding bisproducts, N,N-bis(phosphinoylmethyl)amines were also synthesized under appropriate conditions. The bis(phosphinoyl)amines were then converted to ring platinum complexes after double deoxygenation. The substituent dependence of the energetics of the complexation reaction using bidentate P-ligands, and the stereostructure of a few complexes were evaluated by B3LYP/6-31G(d,p) calculations using the effective core potential (ECP) basis set (SDD). The crystal structure of a few ring Pt species was studied by X-ray analysis. Catalytic activity of the complexes synthesized was investigated in hydroformylation.