Provided herein are diaryl and arylalkyl phosphonates, useful as intermediates in, for example, the synthesis of leukocyte elastase inhibitors, potassium channel modulators, chemiluminescence materials, and flame retardants, and methods for making same. Also provided are N-heterocyclic phosphorodiamidic acids (NHPAs) useful in reactions such as, for example, in the preparation of diaryl and arylalkyl phosphonates. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

The present specification provides a method of preparing a heterogeneous linear carbonate, including transesterifying an aliphatic alcohol and a symmetric linear carbonate in the presence of a catalyst, wherein the catalyst is a porous type basic ion exchange resin having an exchange capacity of 1 (eq/l-wet resin) or more and 1.5 (eq/l-wet resin) or less. The preparation method of the present specification provides a method of preparing a heterogeneous, symmetric linear carbonate and asymmetric linear carbonate in high yield without a process of reactive distillation.

A method of preparing bio-polyols from epoxidized fatty acid esters, wherein the bio-polyols are synthesized via hydroxylation with epoxidized fatty acid esters and ring-opening reagent, using the acidic ionic liquids as catalysts. The bio-polyols are used to synthesize bio-polyurethane and bio-polyurethane foams. The acidic ionic liquids in this process is used in esterification, epoxidation, and ring-opening reaction to synthesize bio-polyols. The ionic liquids catalysts have several advantages such as easy to separate, reusable, and may reduce pollution.

A method for dehydrocoupling silanes and amines. The method comprises contacting: (a) an aliphatic amine; (b) a silane; and (c) a catalyst which is Z.sub.nX.sub.2, wherein X is alkyl, chloride, bromide, iodide, trifluoromethanesulfonate, bis(trifluoromethane)sulfonamide, tosylate, methanesulfonate or O.sub.3S(CF.sub.2)XCF.sub.3 wherein x is an integer from 1 to 10.

The present disclosure provides a method for preparing o-phenyl phenoxyalkyl acrylate, including: transesterifying an acrylate-based compound with a biphenyl alcohol compound in the absence of a solvent and in the presence of a catalyst and a polymerization inhibitor to prepare the o-phenyl phenoxyalkyl acrylate represented by the following formula (II),

##STR00001##

wherein the catalyst is a compound containing a tin element or a titanium element. According to the method of the present disclosure, the o-phenyl phenoxyalkyl acrylate having transparency and high refractive index can be obtained. Moreover, the method of the present disclosure has the characteristics of high conversion rate and high selectivity, and does not need to add other organic solvents, so that many purification processes can be saved, and the production cost is effectively reduced, which has the value of industrial application.

The present disclosure provides a method for preparing o-phenyl phenoxyalkyl acrylate, including: transesterifying an acrylate-based compound with a biphenyl alcohol compound in the absence of a solvent and in the presence of a catalyst and a polymerization inhibitor to prepare the o-phenyl phenoxyalkyl acrylate represented by the following formula (II), ##STR00001##
wherein the catalyst is a compound containing a tin element or a titanium element. According to the method of the present disclosure, the o-phenyl phenoxyalkyl acrylate having transparency and high refractive index can be obtained. Moreover, the method of the present disclosure has the characteristics of high conversion rate and high selectivity, and does not need to add other organic solvents, so that many purification processes can be saved, and the production cost is effectively reduced, which has the value of industrial application.

The invention relates to a process for preparing isocyanate containing alkoxysilane groups, in which, in the sequence of steps A) to D), A) alkoxysilano(cyclo)alkylamine is reacted with dialkyl carbonate in the presence of a basic catalyst to give alkoxysilano(cyclo)alkylurethane, B) simultaneously or successively, the catalyst is removed and/or deactivated, and low boilers, solids, salt burdens and/or high boilers are removed, C) alkoxysilano(cyclo)alkylurethane obtained after B) is thermally cleaved to release isocyanate containing alkoxysilane groups and by-product, leaving bottoms material, and D) isocyanate containing alkoxysilane groups and by-product are separated from one another and from bottoms material and collected, wherein the basic catalyst is a guanidine base.

A naphthalenedicarboxylic acid dichloride production method includes causing a reaction between naphthalenedicarboxylic acid and a chlorinating agent at a reaction temperature of 20 C. or higher and 75 C. or lower in presence of a solvent including tetrahydrofuran. The causing a reaction in the naphthalenedicarboxylic acid dichloride production method is preferably performed in presence of N,N-disubstituted formamide.

Controlled release polyurea microcapsules can be prepared from a combination of polyisocyanates using emulsion polymerization. Encapsulated catalysts prepared using the polyurea microcapsules can be used to control the cure rate of coatings and sealants.

Disclosed are compounds of formulae: ##STR00001##
and salts, hydrates, or solvates thereof, where R.sub.1, R.sub.2, R.sub.3, R.sub.5, and R.sub.6 are defined herein, compositions containing these compounds, methods of preparing these compounds, and methods of using these compounds in a variety of applications, such as a surfactant or additive in personal care products.