Gauri Sankar Lal - Whitehall PA Kathryn Sue Hayes - Plymouth Meeting PA
Assignee:
Air Products and Chemicals, Inc. - Allentown PA
International Classification:
C07C 2522
US Classification:
570143
Abstract:
A method of preparing vicinal difluoro aromatic compounds in high yield from hydroxy aromatic compounds and a method of preparing intermediates thereof. The hydroxy aromatic compound can be a mono-, bi- or tricyclic aromatic in which the rings are separate or fused. One or more of the rings can contain heteroatoms, such as oxygen, nitrogen, or sulfur, and can contain one or more substitutions, in addition to the hydroxy substitution.
Synthesis Of Vicinal Difluoro Aromatics And Intermediates Thereof
Gauri Sankar Lal - Whitehall PA Kathryn Sue Hayes - Plymouth Meeting PA
Assignee:
Air Products and Chemicals, Inc. - Allentown PA
International Classification:
C07C 2522
US Classification:
570143
Abstract:
A method of preparing vicinal difluoro aromatic compounds in high yield from hydroxy aromatic compounds and a method of preparing intermediates thereof. The hydroxy aromatic compound can be a mono-, bi- or tricyclic aromatic in which the rings are separate or fused. One or more of the rings can contain heteroatoms, such as oxygen, nitrogen, or sulfur, and can contain one or more substitutions, in addition to the hydroxy substitution.
Synthesis Of Vicinal Difluoro Aromatics And Intermediates Thereof
Gauri Sankar Lal - Whitehall PA Kathryn Sue Hayes - Plymouth Meeting PA
Assignee:
Air Products and Chemicals, Inc. - Allentown PA
International Classification:
C07C 2522
US Classification:
570123, 570143
Abstract:
A method of preparing vicinal difluoro aromatic compounds in high yield from hydroxy aromatic compounds and a method of preparing intermediates thereof. The hydroxy aromatic compound can be a mono-, bi- or tricyclic aromatic in which the rings are separate or fused. One or more of the rings can contain heteroatoms, such as oxygen, nitrogen, or sulfur, and can contain one or more substitutions, in addition to the hydroxy substitution.
Synthesis Of Vicinal Difluoro Aromatics And Intermediates Thereof
Axel Klauck-Jacobs - Whitehall PA, US Kathryn Sue Hayes - Plymouth Meeting PA, US Reiner Taege - Heiligenhaus, DE William Casteel - Emmaus PA, US Gauri Sankar Lal - Whitehall PA, US
Assignee:
Air Products and Chemicals, Inc. - Allentown PA
International Classification:
C07C025/22
US Classification:
570143, 570123
Abstract:
A method of preparing vicinal difluoro aromatic compounds in high yield from hydroxy aromatic compounds using various bases and a method of preparing intermediates thereof. A method for making a vicinal difluoro halogenated aromatic compound including providing a tetrafluoro derivative of a halogen substituted aromatic compound, wherein the tetrafluoro derivative has two fluorine atoms on each of two adjacent carbons and at least one additional halogen substituent; reacting the tetrafluoro derivative with a reducing agent in presence of a base for a reaction time sufficient to form the vicinal difluoro halogenated aromatic compound containing two vicinal fluorine substituents and the at least one additional halogen substituent, wherein the reducing agent is used in a reducing agent effective amount sufficient to retain the at least one additional halogen substituent.
Process For Producing 1,1-Difluorovinyl Cycloaliphatic Compounds
This invention relates to a process for the preparation of 1,1-difluoroolefins, e. g. , difluorovinyl cycloaliphatic compounds such as difluorovinylcyclohexane and derivatives by the dehydrofluorination of a trifluoromethyl-substituted cycloaliphatic compound and the resulting compositions. This method utilizes a “sterically hindered super-base” system represented by the formula MNRR; where M is Na or K and R is a secondary, or tertiary alkyl or cycloalkyl group of amines for effecting dehydrofluorination of the trifluoromethyl group leading to the difluorovinyl based cycloaliphatic compounds. The sterically hindered super base can be formed by the, in situ, reaction of a sodium or potassium alkoxide, e. g. , KtBuO with a lithium dialkylamide where the lithium is bonded to nitrogen atom of an amine bearing secondary or tertiary aliphatic groups.
Process For Hydrogenation Of Cyanopropionaldehyde-Containing Cyanopropionadelhyde Acetals
Gamini Ananda Vedage - Bethlehem PA Kathryn Sue Hayes - Norristown PA
Assignee:
Air Products and Chemicals, Inc. - Allentown PA
International Classification:
C07C20948
US Classification:
564490
Abstract:
Disclosed is an improved process for the catalytic hydrogenation of cyanopropionaldehyde alkyl acetals (CPAA) to form the aminobutyraldehyde alkyl acetals. The basic process comprises hydrogenating the cyanopropionaldehyde alkyl acetals by contacting said cyanopropionaldehyde alkyl acetals with hydrogen in the presence of a nickel or cobalt catalyst under conditions for reducing the nitrile group to the primary amine. The improvement resides in effecting the hydrogenation of a cyanopropionitrile dialkyl acetal feedstock containing contaminating levels of cyanopropionaldehyde in the presence of a secondary alkanol or water.
Multi-Metallic Actalysts For Amination Of Alcohols To Form Alkylamines
Gamini Ananda Vedage - Bethlehem PA Kathryn Sue Hayes - Norristown PA Malee Leeaphon - Allentown PA John Nelson Armor - Orefield PA
Assignee:
Air Products and Chemicals, Inc. - Allentown PA
International Classification:
C07C20938
US Classification:
564480
Abstract:
A process for the production of aliphatic amines by reacting aliphatic alcohols with an amino compound in the presence of a catalyst containing at least two inter-dispersed metals, in a multi-metallic structure, in which at least one of the metals is nickel or cobalt, and at least one other metal is palladium, platinum, rhodium, ruthenium, or copper.
Amidoamine And Polyamide Curing Agents, Compositions, And Methods
- Allentown PA, US Shiying ZHENG - Center Valley PA, US Kathryn Sue HAYES - Plymouth Meeting PA, US
International Classification:
C08G 59/54 C08G 59/24 C08G 59/44
Abstract:
A composition including an amidoamine curing agent composition or a polyamide curing agent composition are disclosed. The composition includes the reaction products of (1) an amine component including at least one multifunctional amine of structure (I):wherein each R is independently H or CHCHCHNH; Ris H, CHCHCHN—, C1-C21 alkyl, or C1-C21 alkenyl; n is 2; and m is 1 or 2, with (2) a fatty acid or ester component selected from the group consisting of a dimer fatty acid or ester component, a monofunctional fatty acid or ester component, and combinations thereof. The amidoamine curing agent composition remains as liquid at ambient temperature.
Dr. Hayes graduated from the University of Kansas School of Medicine in 1991. She works in McPherson, KS and 1 other location and specializes in Family Medicine. Dr. Hayes is affiliated with Mercy Hospital.
OB/GYN Associates Oak RidgeObstetrics & Gynecology Associates Of Oak Ridge PC 988 Oak Rdg Tpke STE 140, Oak Ridge, TN 37830 (865)4837415 (phone), (865)4837980 (fax)
Education:
Medical School University of Tennessee College of Medicine at Memphis Graduated: 2006
Abnormal Vaginal Bleeding Candidiasis of Vulva and Vagina Complicating Pregnancy or Childbirth Herpes Genitalis Polycystic Ovarian Syndrome (PCOS)
Languages:
English Spanish
Description:
Dr. Hayes graduated from the University of Tennessee College of Medicine at Memphis in 2006. She works in Oak Ridge, TN and specializes in Obstetrics & Gynecology. Dr. Hayes is affiliated with Methodist Medical Center.
Rose Hill Elementary School Kirkland WA 1964-1966, Finn Hill Junior High School Kirkland WA 1968-1969, Lake Washington High School Kirkland WA 1970-1974
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