The present invention describes a new alkynylation and cyanation agent, as well as its preparation and use to introduce nitrile (cyano) or alkyne groups into chemical target molecules by means of an electrophilic reaction. To enable an electrophilic reaction, the chemical backbone of dibenzothiophene was used.

The present invention describes a new alkynylation and cyanation agent, as well as its preparation and use to introduce nitrile (cyano) or alkyne groups into chemical target molecules by means of an electrophilic reaction. To enable an electrophilic reaction, the chemical backbone of dibenzothiophene was used.

The present invention relates to a preheating process and a start-up process for the ammoxidation reaction. The preheating process or the start-up process at least includes the step of heating the catalyst bed in the ammoxidation reactor while controlling the reactor operation linear speed to 0.03-0.15 m/s. The start-up process of the present invention has the advantages such as the significantly reduced launch time compared with the prior art and the operation safety.

The present invention relates to a preheating process and a start-up process for the ammoxidation reaction. The preheating process or the start-up process at least includes the step of heating the catalyst bed in the ammoxidation reactor while controlling the reactor operation linear speed to 0.03-0.15 m/s. The start-up process of the present invention has the advantages such as the significantly reduced launch time compared with the prior art and the operation safety.

The present invention relates to a preheating process and a start-up process for the ammoxidation reaction. The preheating process or the start-up process at least includes the step of heating the catalyst bed in the ammoxidation reactor while controlling the reactor operation linear speed to 0.03-0.15 m/s. The start-up process of the present invention has the advantages such as the significantly reduced launch time compared with the prior art and the operation safety.

The present invention relates to a preheating process and a start-up process for the ammoxidation reaction. The preheating process or the start-up process at least includes the step of heating the catalyst bed in the ammoxidation reactor while controlling the reactor operation linear speed to 0.03-0.15 m/s. The start-up process of the present invention has the advantages such as the significantly reduced launch time compared with the prior art and the operation safety.

The present invention relates to a novel process for preparing and isolating 3,4-dichloro-N-(2-cyanophenyl)-5-isothiazolecarboxamide (Isotianil), which can be used as an active compound with microbicidal properties, wherein the amount of waste materialse.g. solvents and diluentsis significantly reduced and the process meets the requirements of industrial scale production, in particular that it provides the product in high yield, high purity, i.e. minimum amount of by-products and impurities, and can be carried out with tolerable corrosivity in industrial scale metal, in particular stainless steel, vessels or CrNiMo alloy pressure filters or centrifuges.

A process for producing unsaturated nitrile, using a fluidized bed reactor and comprising a reaction step of subjecting hydrocarbon to a vapor phase catalytic ammoxidation reaction in the presence of a catalyst to produce the corresponding unsaturated nitrile, wherein when an internal space of the reactor is divided into two spaces of an upper space occupying a space from an upper end of an inlet of a cyclone to an upper end of the internal space and a lower space occupying a space below the upper end of the inlet of the cyclone and ranging to a dispersion plate, a ratio of an existing amount of the catalyst in the upper space to an existing amount of the catalyst in the lower space is 0.05 to 0.45 in the reaction step.

A process for producing unsaturated nitrile, using a fluidized bed reactor and comprising a reaction step of subjecting hydrocarbon to a vapor phase catalytic ammoxidation reaction in the presence of a catalyst to produce the corresponding unsaturated nitrile, wherein when an internal space of the reactor is divided into two spaces of an upper space occupying a space from an upper end of an inlet of a cyclone to an upper end of the internal space and a lower space occupying a space below the upper end of the inlet of the cyclone and ranging to a dispersion plate, a ratio of an existing amount of the catalyst in the upper space to an existing amount of the catalyst in the lower space is 0.05 to 0.45 in the reaction step.

Described herein are improved chemical reactors for carrying out partial oxidation reactions. The chemical reactor permits the use of levels of oxygen above the lower explosion limit (LEL) typically used in partial oxidation reactions, which increases both volumetric reactivity and conversion per pass, resulting in reduced separation and reactant recycle costs. Also described are methods of using the reactors.