C07C37/08

THE OPTIMIZATION OF O-SULFONATED PHENOL PRODUCTION FOR CUMENE HYDROPEROXIDE CLEAVAGE

A method for the manufacture of a sulfonated phenol for use as a cumene hydroperoxide decomposition catalyst can comprise: combining phenol and a sulfonating agent at a first temperature that is 1 C. to 15 C. higher than a melting temperature of the phenol, to form a reaction mixture at the first temperature; reducing the first temperature of the reaction mixture to a second temperature that is 10 to 40 C. lower than the first temperature; and forming the sulfonated phenol at the second temperature.

THE OPTIMIZATION OF O-SULFONATED PHENOL PRODUCTION FOR CUMENE HYDROPEROXIDE CLEAVAGE

A method for the manufacture of a sulfonated phenol for use as a cumene hydroperoxide decomposition catalyst can comprise: combining phenol and a sulfonating agent at a first temperature that is 1 C. to 15 C. higher than a melting temperature of the phenol, to form a reaction mixture at the first temperature; reducing the first temperature of the reaction mixture to a second temperature that is 10 to 40 C. lower than the first temperature; and forming the sulfonated phenol at the second temperature.

METHOD FOR PRODUCING MODIFIED ALUMINOSILICATE, MODIFIED ALUMINOSILICATE, AND METHOD FOR PRODUCING AROMATIC POLYHYDROXIDE COMPOUND USING SAME

Provided is a method for manufacturing a modified aluminosilicate in which a hydroquinone is highly selectively manufactured by a reaction between a phenol and hydrogen peroxide under industrially advantageous conditions, wherein the manufacturing method includes: a second step for treating an aluminosilicate with an acid; a third step for performing primary calcination of the treatment product obtained in the second step; and a fourth step in which the primary calcined product obtained in the third step and liquid containing one or more elements selected from the group consisting of elements in Group 4 and Group 5 of the Periodic Table are brought into contact with each other, and drying and secondary calcination then performed.

METHOD FOR PRODUCING MODIFIED ALUMINOSILICATE, MODIFIED ALUMINOSILICATE, AND METHOD FOR PRODUCING AROMATIC POLYHYDROXIDE COMPOUND USING SAME

Provided is a method for manufacturing a modified aluminosilicate in which a hydroquinone is highly selectively manufactured by a reaction between a phenol and hydrogen peroxide under industrially advantageous conditions, wherein the manufacturing method includes: a second step for treating an aluminosilicate with an acid; a third step for performing primary calcination of the treatment product obtained in the second step; and a fourth step in which the primary calcined product obtained in the third step and liquid containing one or more elements selected from the group consisting of elements in Group 4 and Group 5 of the Periodic Table are brought into contact with each other, and drying and secondary calcination then performed.

Chromium-catalyzed production of alcohols from hydrocarbons

Processes for converting a hydrocarbon reactant into an alcohol compound and/or a carbonyl compound are disclosed, and these processes include the steps of forming a supported chromium catalyst comprising chromium in a hexavalent oxidation state, irradiating the hydrocarbon reactant and the supported chromium catalyst with a light beam at a wavelength in the UV-visible spectrum to reduce at least a portion of the supported chromium catalyst to form a reduced chromium catalyst, and hydrolyzing the reduced chromium catalyst to form a reaction product comprising the alcohol compound and/or the carbonyl compound. The supported chromium catalyst can be formed by heat treating a supported chromium precursor, contacting a chromium precursor with a solid support while heat treating, or heat treating a solid support and then contacting a chromium precursor with the solid support.

Cyclohexylbenzene composition

Disclosed is (i) a process of making phenol and/or cyclohexanone from cyclohexylbenzene including a step of removing methylcyclopentylbenzene from (a) the cyclohexylbenzene feed supplied to the oxidation step and/or (b) the crude phenol product (ii) a phenol composition and (iii) a cyclohexylbenzene composition that can be made using the process.

Cyclohexylbenzene composition

Disclosed is (i) a process of making phenol and/or cyclohexanone from cyclohexylbenzene including a step of removing methylcyclopentylbenzene from (a) the cyclohexylbenzene feed supplied to the oxidation step and/or (b) the crude phenol product (ii) a phenol composition and (iii) a cyclohexylbenzene composition that can be made using the process.

Cyclohexylbenzene composition

Disclosed is (i) a process of making phenol and/or cyclohexanone from cyclohexylbenzene including a step of removing methylcyclopentylbenzene from (a) the cyclohexylbenzene feed supplied to the oxidation step and/or (b) the crude phenol product (ii) a phenol composition and (iii) a cyclohexylbenzene composition that can be made using the process.

Optimization of O-sulfonated phenol production for cumene hydroperoxide cleavage

A method for the manufacture of a sulfonated phenol for use as a cumene hydroperoxide decomposition catalyst can comprise: combining phenol and a sulfonating agent at a first temperature that is 1 C. to 15 C. higher than a melting temperature of the phenol, to form a reaction mixture at the first temperature; reducing the first temperature of the reaction mixture to a second temperature that is 10 to 40 C. lower than the first temperature; and forming the sulfonated phenol at the second temperature.

Optimization of O-sulfonated phenol production for cumene hydroperoxide cleavage

A method for the manufacture of a sulfonated phenol for use as a cumene hydroperoxide decomposition catalyst can comprise: combining phenol and a sulfonating agent at a first temperature that is 1 C. to 15 C. higher than a melting temperature of the phenol, to form a reaction mixture at the first temperature; reducing the first temperature of the reaction mixture to a second temperature that is 10 to 40 C. lower than the first temperature; and forming the sulfonated phenol at the second temperature.