This invention relates to a preparation method of an ester compound that can reduce energy consumption due to convenient post-treatment process, and simultaneously, can produce products of high purities.

This invention relates to a preparation method of an ester compound that can reduce energy consumption due to convenient post-treatment process, and simultaneously, can produce products of high purities.

Provided is a method of preparing a diester-based material, more particularly, a method of preparing a diester-based material, which is carried out by a continuous preparation process of a diester-based material including a reaction part in which a total of n reaction units from a first reaction unit to an nth reaction unit are connected in series, the reaction unit including a reactor which esterifies dicarboxylic acid and alcohol, including: esterifying dicarboxylic acid and alcohol in a reactor of the first reaction unit to produce a reaction product, and supplying a lower discharge stream including the reaction product to a reaction unit at a rear end through a lower discharge line; and supplying a liquid material through a liquid supply line connected to a lower discharge line of the reactor of the first reaction unit.

Provided is a method of preparing a diester-based material, more particularly, a method of preparing a diester-based material, which is carried out by a continuous preparation process of a diester-based material including a reaction part in which a total of n reaction units from a first reaction unit to an nth reaction unit are connected in series, the reaction unit including a reactor which esterifies dicarboxylic acid and alcohol, including: esterifying dicarboxylic acid and alcohol in a reactor of the first reaction unit to produce a reaction product, and supplying a lower discharge stream including the reaction product to a reaction unit at a rear end through a lower discharge line; and supplying a liquid material through a liquid supply line connected to a lower discharge line of the reactor of the first reaction unit.

The present invention relates to a stripping method capable of recovering, by an environmentally friendly method, a high-purity ester-based compound without concern over the oxidation of an ester-based compound from a mixture containing the ester-based compound. The stripping method has advantages of generating no wastewater, enabling equipment costs to be reduced by simplifying the process, removing concern over the oxidation of an ester-based compound during the process, and enabling the reuse of the components recovered in the process.

The present invention relates to a stripping method capable of recovering, by an environmentally friendly method, a high-purity ester-based compound without concern over the oxidation of an ester-based compound from a mixture containing the ester-based compound. The stripping method has advantages of generating no wastewater, enabling equipment costs to be reduced by simplifying the process, removing concern over the oxidation of an ester-based compound during the process, and enabling the reuse of the components recovered in the process.

The present invention relates to a process for the preparation of dimethyl fumarate, a compound of formula I, in a purity of at least 99.0% as determined by HPLC, containing less than 400 ppm of an anion of a mineral acid and less than 5 ppm of dimethyl maleate.

A transesterification catalyst that is heterogeneous and a method for preparing said transesterification catalyst are provided. The catalyst can be used in a variety of transesterification reactor configurations including CSTR (continuous stirred tank reactors), ebullated (or ebullating) beds or any other fluidized bed reactors, and PFR (plug flow, fixed bed reactors). The catalyst can be used for manufacturing commercial grade biodiesel, biolubricants and glycerin.

A transesterification catalyst that is heterogeneous and a method for preparing said transesterification catalyst are provided. The catalyst can be used in a variety of transesterification reactor configurations including CSTR (continuous stirred tank reactors), ebullated (or ebullating) beds or any other fluidized bed reactors, and PFR (plug flow, fixed bed reactors). The catalyst can be used for manufacturing commercial grade biodiesel, biolubricants and glycerin.

The present invention relates to kinetic resolution of racemic δ-hydroxyl ester via asymmetric catalytic hydrogenation and an application thereof. In the presence of chiral spiro pyridyl phosphine ligand Iridium catalyst and base, racemic δ-hydroxyl esters were subjected to asymmetric catalytic hydrogenation to obtain extent optical purity chiral δ-hydroxyl esters and corresponding 1,5-diols. The method is a new, efficient, highly selective, economical, desirably operable and environmentally friendly method suitable for industrial production. An optically active chiral δ-hydroxyl ester and 1,5-diols can be obtained at very high enantioselectivity and yield with relatively low usage of catalyst. The chiral δ-hydroxyl ester and 1,5-diols obtained by using the method can be used as a critical raw material for asymmetric synthesis of chiral drugs (R)-lisofylline and natural drugs (+)-civet, (−)-indolizidine 167B and (−)-coniine.