Atlantic Richfield Company

Jar-lin Kao

Ming N Sheng

John J Leonard

Gregory A Wheaton

Harold Shalit

A process for the preparation of bromoalkyl esters and vicinal glycol esters which comprises thermally decomposing at temperatures of from 100.degree. C. to 200.degree. C. a bis(2-bromoalkyl)tellurium dicarboxylate compound of the formula ##STR1## wherein at least one R is hydrogen or R is a methyl group and R' is hydrogen or an alkyl group having 1 to 3 carbon atoms in the presence of an aliphatic monocarboxylic acid selected from formic, acetic, propionic or butyric acid employed as solvent and to facilitate solvolysis in the reaction to give in addition to the bromoalkyl ester, the vicinal glycol ester. An inert acetonitrile solvent may be employed alone to give predominately the bromoalkyl ester or an admixture with the acid may be employed. Oxygen is preferably employed with the carboxylic acid solvent to provide an increase in the mole ratio of vicinal glycol ester to the bromoalkyl ester produced.

Preparation of esters by the thermal decomposition of a

A process for the preparation of 2-bromoalkyl esters and vicinal glycol esters which comprises thermally decomposing at temperatures of from 100.degree. C. to 200.degree. C. an organic bromoalkyl tellurium compound selected from 2-bromoalkyltellurium tribromide or bis(2-bromoalkyl)tellurium dibromide, wherein the alkyl group is ethyl, propyl or butyl, in a carboxylic acid having from 1 to 4 carbon atoms which is employed as solvent as well as to supply the ester moiety to the esters produced. The esters may be converted to the respective glycol with water or an aqueous base.

Preparation of esters from organic bromo alkyl tellurium compounds

A process for the preparation of a cyclic alkylene carbonate ester which comprises reacting in a liquid phase a cyclic or linear olefin having from 2 to 15 carbon atoms with carbon dioxide at a temperature of from 30.degree. to 160.degree. C., at a total pressure of from 100 to about 2,000 psig and a pH value of between about 4 and 8, in the presence of oxygen or an oxygen-containing gas and a catalytic amount of a mixture of (a) iodine or an iodide of a metal selected from Groups IA, IB, IIA, IIB, VB, VIIB and VIII of the Periodic Table of Elements, (b) a carbonate of a metal selected from Groups IB, IIA, IIB and VIII of the Periodic Table of Elements, (c) a catalytic iron compound and (d) a catalytic soluble cupric salt, and recovering resulting cyclic alkylene carbonate ester.

Preparation of alkylene carbonates from olefins

Phenyl acetic acid is prepared by the reaction of molecular oxygen and the combination of acetic acid and benzene in the presence of a catalytic system featuring both tellurium and halide, the unit atomic ratio of halide to tellurium being within a range from about 3 to about 20, at a temperature within a range from about 100.degree. C. to about 200.degree. C. at a pressure within a range from about 1 to about 15 atmospheres.

Phenyl acetic acid preparation

A process for the preparation of alkylene carbonates having from 3 to 31 carbon atoms per molecule of the general formula ##STR1## which comprises reacting in the liquid phase the corresponding alkylene iodohydrin having from 2 to 30 carbon atoms per molecule with carbon dioxide in the presence of oxygen or an oxygen-containing gas and an effective amount of a catalytic mixture of

Preparation of alkylene carbonates from alkylene iodohydrins

A process for the preparation of a cyclic alkylene carbonate ester which comprises reacting in a liquid phase a cyclic or linear olefin having from 2 to 15 carbon atoms with carbon dioxide at a temperature of from 50 to 160.degree. C., at a total pressure of from 200 to about 2,000 psig and a pH value of between about 4 and 8, in the presence of oxygen or an oxygen-containing gas and a catalytic amount of a mixture of (a) iodine or an iodide of a metal selected from Groups IA, IB, IIA, IIB, VB, VIIB and VIII of the Periodic Table of Elements and (b) a catalytic iron compound, copper compound of mixture thereof deposited on an inert supporting material, and recovering resulting cyclic alkylene carbonate ester.

Process for the liquid phase oxidation of an unsaturated lower aliphatic aldehyde to the corresponding carboxylic acid wherein the oxidation is carried out by passage of an oxygen-containing gas through a liquid medium containing the unsaturated aldehyde and a fluorine-containing organic compound.

Liquid phase oxidation of unsaturated aldehydes to corresponding acids

A process for the preparation of acrylic acid or methacrylic acid by the ruthenium and/or osmium catalyzed conversion of peroxide (peroxy) intermediate compounds, derived from the autoxidation of acrolein or methacrolein, to the corresponding .alpha.,.beta.-unsaturated carboxylic acid, particularly the conversion of permethacrylic acid and methacrolein monopermethacrylate to methacrylic acid.

Catalyzed decomposition of peroxide intermediates resulting from the

A process for the liquid phase oxidation of .alpha.,.beta.-unsaturated aliphatic aldehydes, such as methacrolein and the in situ decomposition or conversion of unsaturated peroxy (peroxide) compounds formed during the oxidation to the corresponding .alpha.,.beta.-unsaturated aliphatic carboxylic acids which comprises passing oxygen or an oxygen-containing gas such as air through an inert solvent solution of the unsaturated aldehyde at a suitable temperature and pressure in the presence of an organic or inorganic zinc salt catalyst.

Process for the liquid phase oxidation of .alpha.,.beta.-unsaturated

A process for the preparation of acrylic acid or methacrylic acid which comprises catalytically decomposing or converting in the presence of tellurium the peroxide (peroxy) compounds contained in the oxidate solution derived from the autoxidation of acrolein or methacrolein, particularly, the conversion of permethacrylic acid and methacrolein monopermethacrylate to methacrylic acid.

Tellurium catalyzed decomposition of peroxide intermediates resulting

A process for the preparation of acrylic acid or methacrylic acid which comprises catalytically decomposing or converting in the presence of selenium the peroxide (peroxy) compounds formed during autoxidation or contained in the oxidate solution derived from the autoxidation of the respective acrolein or methacrolein, particularly, the conversion of permethacrylic acid and methacrolein monopermethacrylate to methacrylic acid.

Selenium catalyzed decomposition of peroxide intermediates resulting

A process for the liquid phase oxidation of .alpha.,.beta.-unsaturated aldehydes, and the in situ decomposition of unsaturated intermediate peroxy (peroxide) compounds formed during oxidation, to the corresponding unsaturated aliphatic acid which comprises passing oxygen or an oxygen-containing gas through an inert solvent solution of the aldehyde at a suitable temperature and pressure in the presence of a catalytic amount of a thallium salt. The solvents employed may be mixed with water forming a heterogeneous solvent system.

Liquid phase oxidation of unsaturated aliphatic aldehydes to unsaturated

A process for the preparation of .alpha.,.beta.-unsaturated aliphatic carboxylic acids by the liquid phase oxidation of the corresponding .alpha.,.beta.-unsaturated aliphatic aldehyde, such as acrolein and methacrolein, and the in situ decomposition or conversion of unsaturated peroxy (peroxide) compounds formed during oxidation, which comprises passing air or oxygen through an inert organic solvent solution of the aldehyde at a suitable temperature and pressure in the presence of a catalytic amount of an organic or inorganic bismuth salt. Heterogeneous solvent systems employing mixtures of the organic solvent and water may be used.

Liquid phase oxidation of unsaturated aldehydes to carboxylic acids with

A method for the production of .alpha.,.beta.-unsaturated aliphatic carboxylic acids by the liquid phase oxidation of the corresponding .alpha.,.beta.-unsaturated aliphatic aldehydes, particularly acrolein and methacrolein, and the in situ decomposition of unsaturated intermediate peroxy (peroxide) compounds formed during oxidation, which comprises passing oxygen or an oxygen-containing gas through an inert solvent solution of the aldehyde at a suitable temperature and pressure in the presence of a catalytic amount of an inorganic or organic antimony salt. The solvent employed may also be mixed with water forming a heterogeneous solvent system.

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Cherry Hill, NJ, United States of America

Jar-lin Kao