C07C2/70

SYNTHESIS OF ARYL COMPOUNDS
20180215687 · 2018-08-02 ·

A method for the synthesis of a aryl compound of Formula (1). Formula (1)


UT-WR.sub.1).sub.n (1)

ALKYLATION PROCESSES USING LIQUID LEWIS ACID CATALYSTS

An alkylation process is described. The alkylation process includes contacting a feed comprising a paraffin or an aromatic with an olefin feed in the presence of a liquid Lewis acid catalyst in an alkylation reaction zone under alkylation conditions to form a reaction mixture comprising alkylation products and the liquid Lewis acid catalyst. The liquid Lewis acid catalyst is the liquid reaction product of a donor molecule and a metal halide. The alkylation products are separated from the liquid Lewis acid catalyst and recovered.

SOLID PHOSPHORIC ACID CATALYSTS

The present disclosure relates to solid phosphoric acid (SPA) catalysts useful in the conversion of hydrocarbons, such as the oligomerization of olefins, to methods for making such SPA catalysts, and to methods for converting hydrocarbons by contacting hydrocarbons with such catalyst. For example, in certain embodiments, the disclosure provides a calcined solid phosphoric acid catalyst composition that includes phosphoric acid and silicon phosphates, and in which (i) one or more promoters each selected from the group consisting of boron, bismuth, tungsten, silver and lanthanum is present; (ii) the composition is a calcined product of a formable mixture including silica-alumina clay, silica fiber and/or silica alumina fiber; or (iii) the composition is a calcined product of a formable mixture including fumed silica.

SOLID PHOSPHORIC ACID CATALYSTS

The present disclosure relates to solid phosphoric acid (SPA) catalysts useful in the conversion of hydrocarbons, such as the oligomerization of olefins, to methods for making such SPA catalysts, and to methods for converting hydrocarbons by contacting hydrocarbons with such catalyst. For example, in certain embodiments, the disclosure provides a calcined solid phosphoric acid catalyst composition that includes phosphoric acid and silicon phosphates, and in which (i) one or more promoters each selected from the group consisting of boron, bismuth, tungsten, silver and lanthanum is present; (ii) the composition is a calcined product of a formable mixture including silica-alumina clay, silica fiber and/or silica alumina fiber; or (iii) the composition is a calcined product of a formable mixture including fumed silica.

Method for producing xylene

A method for producing xylene from feedstock oil includes a cracking/reforming reaction step of bringing the feedstock oil into contact with a catalyst to produce monocyclic aromatic hydrocarbons; a separation/recovery step of separating and recovering, from a product obtained by the cracking/reforming reaction step, a fraction A containing monocyclic aromatic hydrocarbons having a 10 vol % distillation temperature of 75 C. or higher and a 90 vol % distillation temperature of 140 C. or lower, a xylene fraction containing xylene, and a fraction B containing monocyclic aromatic hydrocarbons having a 10 vol % distillation temperature of 145 C. or higher and a 90 vol % distillation temperature of 215 C. or lower; and a xylene conversion step of bringing a mixed fraction obtained by mixing the fractions A and B with each other into contact with a catalyst containing a solid acid to convert the mixed fraction into xylene.

Method for producing xylene

A method for producing xylene from feedstock oil includes a cracking/reforming reaction step of bringing the feedstock oil into contact with a catalyst to produce monocyclic aromatic hydrocarbons; a separation/recovery step of separating and recovering, from a product obtained by the cracking/reforming reaction step, a fraction A containing monocyclic aromatic hydrocarbons having a 10 vol % distillation temperature of 75 C. or higher and a 90 vol % distillation temperature of 140 C. or lower, a xylene fraction containing xylene, and a fraction B containing monocyclic aromatic hydrocarbons having a 10 vol % distillation temperature of 145 C. or higher and a 90 vol % distillation temperature of 215 C. or lower; and a xylene conversion step of bringing a mixed fraction obtained by mixing the fractions A and B with each other into contact with a catalyst containing a solid acid to convert the mixed fraction into xylene.

Synthesis of polycyclic aromatic hydrocarbons

The present invention relates to the synthesis of polycyclic aromatic compounds. Compounds such as terrylene or quaterrylene may now be prepared in relatively high yield by reaction of naphthalene or perylene via Scholl-type coupling in the presence of a superacid and an oxidant in an inert solvent.

Synthesis of polycyclic aromatic hydrocarbons

The present invention relates to the synthesis of polycyclic aromatic compounds. Compounds such as terrylene or quaterrylene may now be prepared in relatively high yield by reaction of naphthalene or perylene via Scholl-type coupling in the presence of a superacid and an oxidant in an inert solvent.

Ethylbenzene Production with Ethylene from Oxidative Coupling of Methane

A method for producing ethylbenzene (EB) comprising introducing to an oxidative coupling of methane (OCM) reactor an OCM reactant mixture comprising CH.sub.4 and O.sub.2; allowing the OCM reactant mixture to react via OCM reaction to form an OCM product mixture comprising C.sub.2H.sub.4, C.sub.2H.sub.6, water, CO, CO.sub.2 and unreacted methane; separating the water and optionally CO and/or CO.sub.2 from the OCM product mixture to yield an EB reactant mixture comprising C.sub.2H.sub.4, C.sub.2H.sub.6, unreacted methane, and optionally CO and/or CO.sub.2; (d) introducing benzene and an EB reactant mixture to an EB reactor; allowing benzene to react in a liquid phase with the ethylene of the EB reactant mixture to form EB; recovering from the EB reactor an EB product mixture comprising EB and unreacted benzene, and an unreacted alkanes mixture comprising C.sub.2H.sub.6 and unreacted methane, and optionally CO and/or CO.sub.2; and optionally recycling the unreacted alkanes mixture to the OCM reactor.

Method for separating 2-alkylanthracenes and use thereof for producing hydrogen peroxide

A method for preparing 2-alkylanthracene includes the step of separating 2-alkylanthracene from a reaction product of anthracene alkylation reaction. The anthracene alkylation reaction is a reaction of anthracene and an alkylation reagent under an alkylation condition and in the presence of an alkylation reaction solvent and a catalyst. The reaction product of the anthracene alkylation reaction contains anthracene and the product of a series of alkylanthracenes containing 2-alkylanthracene.