C25B3/11

Method for synthesizing beta-cyano ketone compound

Disclosed is a method for synthesizing β-cyano ketone compound, including steps of (1) adding a α-keto acid and sodium hydroxide to a separator-free electrolytic cell, adding acetonitrile thereto, and dissolving the α-keto acid and sodium hydroxide in acetonitrile by stirring to be uniform, to obtain a dissolution solution; (2) adding an alkene or a derivative thereof, cyanobenziodoxolone, and an electrolyte to the dissolution solution, to obtain a mixed solution; (3) subjecting the mixed solution to an electrochemical reaction by electrifying a cathode of a platinum sheet, and an anode of a graphite electrode to obtain a reacted solution; and (4) after the electrochemical reaction, collecting the reacted solution, adding water thereto and stirring to obtain a mixture, subjecting the mixture to an extraction to obtain an organic phase, drying the organic phase and purifying, to obtain the β-cyano ketone compound.

ELECTROCHEMICAL BREAKING OF C-C BONDS
20230106006 · 2023-04-06 ·

Electrochemical systems and methods for cleaving C—C bonds are disclosed. In performing the method, a reactant adsorption electrical potential, a C—C bond breaking electrical potential, and a desorption electrical potential are sequentially applied to an electrode pair contacting a composition initially containing a target chemical reactant, such as a polymer or alkane. As a result of performing the method, one or more desired chemical products, such as smaller alkane-containing molecules, are released from the electrode into the region between the electrode pairs. The method may be performed at ambient temperatures using renewable electricity.

ELECTROSYNTHESIS OF OXIRANES
20230146508 · 2023-05-11 ·

Electrosynthesis of oxirane can include contacting a halide electrolyte with an anode and cathode respectively located in anodic and cathodic compartments; supplying olefin reactants into the electrolyte in the anodic compartment, such that the anode generates ethylene chlorohydrin; withdrawing a loaded anodic solution comprising ethylene halohydrin from the anodic compartment, and a loaded cathodic solution comprising OH.sup.- ions from the cathodic compartment; and mixing the loaded anodic solution with the loaded cathodic solution under conditions to react ethylene halohydrin with OH- to produce oxirane. The electrocatalyst can include iridium oxide on a titanium substrate, with the iridium oxide provided as nanoparticles on a titanium mesh, and the electrolyte can be aqueous KCl. The electrocatalyst can define an extended heterogenous:homogenous interface with halide ions acting as a reservoir for positive charges, thereby storing and redistributing positive charges to promote selective generation of ethylene halohydrins.

CATALYST-FREE ELECTROCHEMICAL DEUTERATION METHOD USING DEUTERIUM OXIDE AS DEUTERIUM SOURCE
20210404070 · 2021-12-30 ·

A catalyst-free electrochemical deuteration method using deuterium oxide as a deuterium source, adding an electrolyte, an organic compound containing an ethylenic bond or acetylenic bond, deuterium oxide, and an organic solvent into a reactor, applying a direct current voltage of 4-8 V between electrodes of a carbon felt in an atmosphere of an inert gas for an electrolytic reaction, to obtain a product, and purifying the product to obtain a deuterated product. In the method provided by the present disclosure, with the organic compound containing an ethylenic bond or acetylenic bond as a raw material, deuterium oxide as a deuterium source, cheap and readily available carbon electrode materials as cathodes and anodes, it is possible to obtain deuterated products by a direct current electrolysis in an organic solvent, without any transition metal catalysts.

CATALYST-FREE ELECTROCHEMICAL DEUTERATION METHOD USING DEUTERIUM OXIDE AS DEUTERIUM SOURCE
20210404070 · 2021-12-30 ·

A catalyst-free electrochemical deuteration method using deuterium oxide as a deuterium source, adding an electrolyte, an organic compound containing an ethylenic bond or acetylenic bond, deuterium oxide, and an organic solvent into a reactor, applying a direct current voltage of 4-8 V between electrodes of a carbon felt in an atmosphere of an inert gas for an electrolytic reaction, to obtain a product, and purifying the product to obtain a deuterated product. In the method provided by the present disclosure, with the organic compound containing an ethylenic bond or acetylenic bond as a raw material, deuterium oxide as a deuterium source, cheap and readily available carbon electrode materials as cathodes and anodes, it is possible to obtain deuterated products by a direct current electrolysis in an organic solvent, without any transition metal catalysts.

ELECTROCHEMICAL, DEHYDROGENATION, EPOXIDATION, SUBSTITUTION, AND HALOGENATION OF HYDROCARBONS AND HYDROCARBON DERIVATIVES

A method of making alkenes and/or epoxides from alkanes and hydroxy-alkanes, respectively. In a reactor having an anode and a cathode separated by an ion exchange membrane, and containing a solution comprising water, halogen ions, and an alkane and/or a hydroxy-alkane, apply a potential across the anode and the cathode such that a halogenated intermediate is produced at the anode as an anolyte and hydroxyl ions are produced at the cathode as a catholyte; and combining the anolyte and the catholyte to yield an alkene and/or an epoxide.

Microfluidic Process for the General Electrochemical Synthesis of Geminal Dipseudohalide or Halide-Pseudohalide Compounds

A process for the microfluidic electrochemical synthesis of geminal dipseudohalide or halide-pseudohalide compounds comprising the steps of pumping a solution comprising a compound of Formula I

##STR00001## into a microfluidic electrochemical reactor in the presence of a base, one of a halide or pseudohalide salt (MY), and a mediator; applying an electrical current through the microfluidic electrochemical reactor; and performing oxidative addition to create a geminal dipseudohalide or halide-pseudohalide compound of the general Formula II

##STR00002##

Microfluidic Process for the General Electrochemical Synthesis of Geminal Dipseudohalide or Halide-Pseudohalide Compounds

A process for the microfluidic electrochemical synthesis of geminal dipseudohalide or halide-pseudohalide compounds comprising the steps of pumping a solution comprising a compound of Formula I

##STR00001## into a microfluidic electrochemical reactor in the presence of a base, one of a halide or pseudohalide salt (MY), and a mediator; applying an electrical current through the microfluidic electrochemical reactor; and performing oxidative addition to create a geminal dipseudohalide or halide-pseudohalide compound of the general Formula II

##STR00002##

Electrochemical, dehydrogenation, epoxidation, substitution, and halogenation of hydrocarbons and hydrocarbon derivatives

A method of making alkenes and/or epoxides from alkanes and hydroxy-alkanes, respectively. In a reactor having an anode and a cathode separated by an ion exchange membrane, and containing a solution comprising water, halogen ions, and an alkane and/or a hydroxy-alkane, apply a potential across the anode and the cathode such that a halogenated intermediate is produced at the anode as an anolyte and hydroxyl ions are produced at the cathode as a catholyte; and combining the anolyte and the catholyte to yield an alkene and/or an epoxide.

Electrochemical, dehydrogenation, epoxidation, substitution, and halogenation of hydrocarbons and hydrocarbon derivatives

A method of making alkenes and/or epoxides from alkanes and hydroxy-alkanes, respectively. In a reactor having an anode and a cathode separated by an ion exchange membrane, and containing a solution comprising water, halogen ions, and an alkane and/or a hydroxy-alkane, apply a potential across the anode and the cathode such that a halogenated intermediate is produced at the anode as an anolyte and hydroxyl ions are produced at the cathode as a catholyte; and combining the anolyte and the catholyte to yield an alkene and/or an epoxide.