C07C29/32

Synthesis of pheromones and related materials via olefin metathesis

Methods for preparation of olefins, including 8- and 11-unsaturated monoenes and polyenes, via transition metathesis-based synthetic routes are described. Metathesis reactions in the methods are catalyzed by transition metal catalysts including tungsten-, molybdenum-, and ruthenium-based catalysts. The olefins include insect pheromones useful in a number of agricultural applications.

METHOD AND CATALYST FOR PRODUCING METHYLBENZYL ALCOHOL FROM ETHANOL BY CATALYTIC CONVERSION
20210246092 · 2021-08-12 ·

The present invention relates to methods and catalysts for producing methylbenzyl alcohol from ethanol by catalytic conversion, and belongs to the field of chemical engineering and technology. The present invention develops a route of producing methylbenzyl alcohol starting from green and sustainable ethanol and provide corresponding catalysts used for the catalytic conversion route. This innovative reaction route has several advantages, such as, simple process, eco-friendly property, and easy separation of products, as compared with a traditional petroleum-based route. This present route has a reaction temperature of 150-450° C. and total selectivity of 72% for methylbenzyl alcohol, and has good industrial application prospect. The innovation of this patent comprises the catalysts synthesis and the reaction route.

METHOD AND CATALYST FOR PRODUCING METHYLBENZYL ALCOHOL FROM ETHANOL BY CATALYTIC CONVERSION
20210246092 · 2021-08-12 ·

The present invention relates to methods and catalysts for producing methylbenzyl alcohol from ethanol by catalytic conversion, and belongs to the field of chemical engineering and technology. The present invention develops a route of producing methylbenzyl alcohol starting from green and sustainable ethanol and provide corresponding catalysts used for the catalytic conversion route. This innovative reaction route has several advantages, such as, simple process, eco-friendly property, and easy separation of products, as compared with a traditional petroleum-based route. This present route has a reaction temperature of 150-450° C. and total selectivity of 72% for methylbenzyl alcohol, and has good industrial application prospect. The innovation of this patent comprises the catalysts synthesis and the reaction route.

Method for preparation of alkylated or fluoro, chloro and fluorochloro alkylated compounds by heterogeneous cobalt catalysis

The invention discloses a method for preparation of alkylated, fluoro alkylated, chloro alkylated and fluorochloro alkylated compounds by a heterogeneous Co-catalysed alkylation or fluoro, chloro and fluorochloro alkylation with alkyl halides, fluoro alkyl halides, chloro alkyl halides or fluorochloro alkyl halides respectively.

Method for preparation of alkylated or fluoro, chloro and fluorochloro alkylated compounds by heterogeneous cobalt catalysis

The invention discloses a method for preparation of alkylated, fluoro alkylated, chloro alkylated and fluorochloro alkylated compounds by a heterogeneous Co-catalysed alkylation or fluoro, chloro and fluorochloro alkylation with alkyl halides, fluoro alkyl halides, chloro alkyl halides or fluorochloro alkyl halides respectively.

Process for the conversion of synthesis gas to isobutanol

An improved isobutanol synthesis process is provided which proceeds through the formation of mixed alcohols from syngas. The two-step process avoids the slowest -carbon addition reaction in the conventional one-step, direct isobutanol synthesis process. Once ethanol and propanol are produced in the first reaction zone, they can react with methanol and/or syngas in a second reaction zone to produce isobutanol through the fast -carbon addition reaction in the presence of catalysts, resulting on significantly improved isobutanol productivity.

Process for the conversion of synthesis gas to isobutanol

An improved isobutanol synthesis process is provided which proceeds through the formation of mixed alcohols from syngas. The two-step process avoids the slowest -carbon addition reaction in the conventional one-step, direct isobutanol synthesis process. Once ethanol and propanol are produced in the first reaction zone, they can react with methanol and/or syngas in a second reaction zone to produce isobutanol through the fast -carbon addition reaction in the presence of catalysts, resulting on significantly improved isobutanol productivity.

Method of converting ethanol to higher alcohols

A method and catalyst for forming higher alcohols from lower alcohol feedstocks. In one application a highly selective and stable copper pseudo-single-atom supported on MgOAl.sub.2O.sub.3 catalyst is provided which provides ethanol condensation to higher alcohols at 50% yields and 85% selectivity is demonstrated with stable catalyst lifetime over 500 hours in a continuous flow system. In some applications a Guerbet condensation process is further utilized to yield a higher alcohol at a selectivity of near 90%.

Method of converting ethanol to higher alcohols

A method and catalyst for forming higher alcohols from lower alcohol feedstocks. In one application a highly selective and stable copper pseudo-single-atom supported on MgOAl.sub.2O.sub.3 catalyst is provided which provides ethanol condensation to higher alcohols at 50% yields and 85% selectivity is demonstrated with stable catalyst lifetime over 500 hours in a continuous flow system. In some applications a Guerbet condensation process is further utilized to yield a higher alcohol at a selectivity of near 90%.

Method of converting ethanol to higher alcohols

A method and catalyst for forming higher alcohols from lower alcohol feedstocks. In one application a highly selective and stable copper pseudo-single-atom supported on MgOAl.sub.2O.sub.3 catalyst is provided which provides ethanol condensation to higher alcohols at 50% yields and 85% selectivity is demonstrated with stable catalyst lifetime over 500 hours in a continuous flow system. In some applications a Guerbet condensation process is further utilized to yield a higher alcohol at a selectivity of near 90%.