Hoechst Celanese Corporation

Celanese Gmbh

Celanese International Corporation

Charles B Hilton

Olan S Fruchey

Ahmed M Tafesh

James R Sounik

Kenneth G Davenport

Graham N Mott

Richard Vicari

Mohammad Aslam

George Kvakovszky

Bennett C Ward

Thomas M Kenesson

Edward M De La Garza

Anthony J East

Carrie A Feeney

John R Fritch

Theodore Horlenko

Daniel A Aguilar

Wilson B Ray

Daniel D Lindley

B Frank Wood

Thomas A Curtis

Timothy R Ryan

Michael R Ahern

O Stanley Fruchey

Phillip S Snyder

William J Seeliger

James L Ragan

Kan J Tsai

Thomas L Grantland

Gregory M Adams

Ida L Jones

Macroporous, strong-acid polysiloxane ion exchange resins which have been converted to the silver or mercury form are utilized to remove iodides from non-aqueous organic media. In a particularly preferred method, hexyl iodide is removed from acetic acid.

Method of removing iodides from non-aqueous organic media utilizing silver or mercury exchanged macroporous organofunctional polysiloxane resins

Processes for recovering 4,4'-dimethyl bibenzoate (DMBB) from byproduct streams of dimethyl terephthalate (DMT) production are disclosed. The byproduct streams are treated to produce an overhead stream which includes DMBB. In one aspect of the invention, the overhead product stream is added to an organic solvent under conditions sufficient to rapidly form a suspension of crystallized DMBB. In another aspect of the invention, the overhead is dissolved in an appropriate organic solvent and cooled to form a suspension of DMBB crystals in the solvent. A portion of the suspension is removed, and the remaining portion of the suspension centrifuged to recover DMBB crystals. In still another aspect of the invention, the overhead stream is treated with an organic solvent to form a slurry of DMBB crystals, and the resultant slurry thermally treated to increase the concentration of DMBB crystals therein while also solubilizing any organic contaminants.

Processes for cystallizing 4, 4'-dimethyl bibenzoate (DMBB) recovered

The present invention provides a unique and novel way of producing carbinols such as 4-hydroxyphenylmethylcarbinol (HPMC). In this new process, a ketone such as 4-hydroxyacetophenone (4-HAP) is heated under suitable hydrogenation conditions of temperature and pressure in the presence of a suitable catalyst and a basic material, and for a sufficient period of time to form HPMC.

Process for preparing 4-hydroxyphenylmethylcarbinol

The present invention provides a unique and novel way of producing polyhydroxystyrene which comprises the steps of (a) heating 4-hydroxyacetophenone under suitable hydrogenation conditions of temperature and pressure in the presence of a suitable palladium catalyst and a basic material and for a sufficient period of time to form 4-hydroxyphenylmethylcarbinol; (b) heating 4-hydroxyphenylmethylcarbinol under suitable conditions of temperature and pressure and for a sufficient period of time to form said polyhydroxystyrene.

Process for preparing vinylphenol polymers & copolymers

The present invention provides a unique and novel way of producing carbinols such as 4-hydroxyphenylmethylcarbinol (HPMC). In this new process, a ketone such as 4-hydroxyacetophenone (4-HAP) is heated under suitable hydrogenation conditions of temperature and pressure in the presence of a suitable catalyst and for a sufficient period of time to form HPMC.

The present invention provides a unique and novel way of producing vinyl phenols such as poly(4-hydroxystyrene) (PHS). In this new process, 4-hydroxyphenylmethylcarbinol (HPMC) is heated under suitable conditions of temperature and pressure and for a sufficient period of time to form the poly (4-hydroxystyrene) (PHS).

Process for preparing poly(4-hydroxystyrene)

The present invention provides a unique and novel way of producing polyhydroxystyrene which comprises the steps of (a) heating 4-hydroxyacetophenone under suitable hydrogenation conditions of temperature and pressure in the presence of a suitable palladium catalyst and for a sufficient period of time to form 4-hydroxyphenylmethylcarbinol; (b) heating 4-hydroxyphenylmethylcarbinol under suitable conditions of temperature and pressure and for a sufficient period of time to form said polyhydroxystyrene.

Process for preparing vinylphenol polymers and copolymers

The present invention provides new polymer compositions which contain novel substituted pyrazines or pyrazine derivatives ('NPD') which are functional and have useful application as a monomer (co-monomer) for a variety of high performance polymers such as polyester, polyarylate, polycarbonate, polyetherketones, epoxides, polyimides, polyamides, and polyamides-imides. These NPD have the general formula: ##STR1## wherein R.sub.1, R.sub.2, R.sub.3, and R.sub.4 are defined herein.

Polymer compositions containing substituted pyrazines

Acylamides or amine acylate salts of arylalkanolamines are prepared by reacting an arylisonitrosoalkanone with hydrogen and a carboxylic acid, carboxylic acid anhydride or carboxylic acid ester or mixture thereof in the presence of a transition metal catalyst; optionally the product is converted to the corresponding arylalkanolamine hydrochloride salt by reaction of the acylamide or amine acylate salt of the arylalkanolamine with hydrogen chloride in a C.sub.1 -C.sub.3 alkyl alcohol.

Method for the preparation of arylalkanolamineacylates

Method for the preparation of arylalkanolacylamides

Acid addition salts of arylketoamines are prepared by reacting arylisonitrosoalkanones with hydrogen in the presence of a transition metal catalyst and strong acid in a dipolar aprotic solvent.

Method for the preparation of arylketoamines

N-acetyl-para-aminophenol is prepared by contacting 4-hydroxyacetophenone oxime with a Beckmann rearrangement catalyst in an alkyl alkanoate reaction solvent. An integrated process is disclosed wherein 4-hydroxyacetophenone is reacted with a hydroxylamine salt and a base to obtain 4-hydroxyacetophenone oxime, the oxime product is extracted from the resulting reaction mixture with a substantially water-immiscible solvent, and the mixture of oxime and substantially water-immiscible solvent is contacted with a Beckmann rearrangement catalyst to produce N-acetyl-para-aminophenol. Novel Beckamnn rearrangement catalysts are used to limit by-product formation in the ester solvent.

Production of acetaminophen

A continuous process is provided for the production of 4'-isobutylacetophenone (4-IBAP) comprising feeding liquid hydrogen fluoride (HF) and an acetylating agent into an extractor-reactor to form a first, HF-rich phase containing the acetylating agent, feeding isobutylbenzene (IBB) to the extractor-reactor to form a second, IBB-rich phase which is contacted with said first, HF-rich phase in a manner such that the acetylating agent reacts with IBB to form 4-IBAP which is extracted into the first, HF-rich phase, and a light IBB-rich second phase containing the bulk of unreacted IBB, externally recycling said second, IBB-rich phase to the IBB feed point in combination with fresh IBB to make up for IBB consumed in the reaction and that and dissolved in the HF-rich phase, and withdrawing HF-rich phase containing 4-IBAP from the extractor-reactor.

Growing community of inventors

Corpus Christi, TX, United States of America

Charles B Hilton