C07C68/02

PRODUCTION METHOD OF ASYMMETRIC CHAIN CARBONATE

A method for producing an asymmetric chain carbonate by reacting an alcohol with a halocarbonate ester compound in the presence of a basic magnesium salt.

METHOD FOR PRODUCING FLUORINE-CONTAINING DIALKYL CARBONATE COMPOUNDS

The present invention relates to a method for producing fluorine-containing dialkyl carbonate compounds, which are suitable as non-aqueous solvents for non-aqueous electrolytes used in secondary batteries. When an alkyl chloroformate and an alcohol are reacted in the presence of an ether-containing imidazole derivative base, the reaction can be carried out at room temperature as compared with the prior art, and the products can be separated within a short time from the reactants. This is an economical process, and according to the present invention, it is possible to obtain alkyl carbonates containing fluorine atoms simply and without difficulty in the removal of solvents, salts formed during the reaction, and by-products. Accordingly, the production method of the present invention can be effectively applied to the production of fluorine-containing dialkyl carbonates used for various applications such as electrolytes of lithium ion secondary batteries, medicines and fine chemicals, pesticides, polar aprotic solvents, synthetic lubricating oils and the like.

METHOD FOR PRODUCING FLUORINE-CONTAINING DIALKYL CARBONATE COMPOUNDS

The present invention relates to a method for producing fluorine-containing dialkyl carbonate compounds, which are suitable as non-aqueous solvents for non-aqueous electrolytes used in secondary batteries. When an alkyl chloroformate and an alcohol are reacted in the presence of an ether-containing imidazole derivative base, the reaction can be carried out at room temperature as compared with the prior art, and the products can be separated within a short time from the reactants. This is an economical process, and according to the present invention, it is possible to obtain alkyl carbonates containing fluorine atoms simply and without difficulty in the removal of solvents, salts formed during the reaction, and by-products. Accordingly, the production method of the present invention can be effectively applied to the production of fluorine-containing dialkyl carbonates used for various applications such as electrolytes of lithium ion secondary batteries, medicines and fine chemicals, pesticides, polar aprotic solvents, synthetic lubricating oils and the like.

METHOD FOR PRODUCING FLUORINE-CONTAINING DIALKYL CARBONATE COMPOUNDS

The present invention relates to a method for producing fluorine-containing dialkyl carbonate compounds, which are suitable as non-aqueous solvents for non-aqueous electrolytes used in secondary batteries. When an alkyl chloroformate and an alcohol are reacted in the presence of an ether-containing imidazole derivative base, the reaction can be carried out at room temperature as compared with the prior art, and the products can be separated within a short time from the reactants. This is an economical process, and according to the present invention, it is possible to obtain alkyl carbonates containing fluorine atoms simply and without difficulty in the removal of solvents, salts formed during the reaction, and by-products. Accordingly, the production method of the present invention can be effectively applied to the production of fluorine-containing dialkyl carbonates used for various applications such as electrolytes of lithium ion secondary batteries, medicines and fine chemicals, pesticides, polar aprotic solvents, synthetic lubricating oils and the like.

Process for preparing 3-chloro-2-vinylphenylsulfonates

The present invention relates to a new process for preparing 3-chloro-2-vinylphenylsulfonate derivatives.

Process for preparing 3-chloro-2-vinylphenylsulfonates

The present invention relates to a new process for preparing 3-chloro-2-vinylphenylsulfonate derivatives.

Process for preparing 3-chloro-2-vinylphenylsulfonates

The present invention relates to a new process for preparing 3-chloro-2-vinylphenylsulfonate derivatives.

SYNTHETIC ROUTE TO ANTI-VIRAL AGENTS

The invention provides methods of synthesizing a viral protease inhibitor in high yield, without using expensive catalysts or challenging reaction conditions.

SYNTHETIC ROUTE TO ANTI-VIRAL AGENTS

The invention provides methods of synthesizing a viral protease inhibitor in high yield, without using expensive catalysts or challenging reaction conditions.

SYNTHETIC ROUTE TO ANTI-VIRAL AGENTS

The invention provides methods of synthesizing a viral protease inhibitor in high yield, without using expensive catalysts or challenging reaction conditions.