Bonnie G. McKinnie - Baton Rouge LA Gene C. Robinson - Baton Rouge LA
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
B01J 3112 C08F 450
US Classification:
502153
Abstract:
A process for making mixed dialkylmagnesiums wherein magnesium metal is reacted with ethylene and an alkyl halide in the presence of a hydrocarbon solvent and in a substantially moisture-free and ether-free atmosphere, under relatively high pressure and at a relatively high temperature followed by separation of undissolved solids from the resulting solution. A composition of matter produced by the process comprising dialkylmagnesium compounds having at least four different alkyl groups, a hydrocarbon solvent and a small amount of an alkyl or alkoxy aluminum compound.
Bonnie G. McKinnie - Baton Rouge LA Gene C. Robinson - Baton Rouge LA
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07C14390 C11D 128
US Classification:
260400
Abstract:
An alkali metal or an alkaline earth metal salt of an acyloxybenzenesulfonate of the formula: ##STR1## wherein R is a hydrocarbyl group containing up to 30 carbon atoms selected from alkyl, alkenyl, cycloalkyl, aryl, aralkyl and M is an alkali metal or an alkaline earth metal is prepared by reacting at elevated temperature the corresponding hydroxybenzene sulfonate salt of the formula: ##STR2## with an aryl ester of the formula: ##STR3## wherein R is as defined above.
Aluminum Alkyls And Linear 1-Olefins From Internal Olefins
Robert H. Allen - Baton Rouge LA Keith G. Anderson - Baton Rouge LA Steven P. Diefenbach - Baton Rouge LA Ronny W. Lin - Baton Rouge LA Larry H. Nemec - Baton Rouge LA Andrew D. Overstreet - Baton Rouge LA Gene C. Robinson - Baton Rouge LA
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07F 506
US Classification:
556190
Abstract:
Linear 1-olefins are prepared from internal olefins by (i) reacting them in the presence of an isomerization catalyst and a tri-lower alkyl aluminum so as to cause internal olefin to isomerize to 1-olefins which displace the lower alkyl groups to form a trialkyl aluminum compound in which at least one of the alkyl groups is a linear alkyl derived from the 1-olefin, and, thereafter, (ii) reacting the trialkyl aluminum compound with a 1-olefin so as to displace the linear alkyl from the trialkyl aluminum compound, thereby forming a linear 1-olefin product which is substantially free of internal olefins.
Gene C. Robinson - Baton Rouge LA Bonnie G. McKinnie - Baton Rouge LA
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07F 302
US Classification:
260665R
Abstract:
A composition of matter comprising di-isoamylmagnesium and diethylmagnesium, with an isoamyl: ethyl alkyl group ratio of about 1. 4 to about 4:1, which is soluble in aliphatic, cycloaliphatic, and aromatic hydrocarbon solvents is disclosed, as is a process for making such mixed dialkylmagnesium wherein magnesium metal is reacted with an ethyl halide and an isoamyl halide in the presence of the hydrocarbon solvent and in a substantially moisture-free and ether-free atmosphere, followed by separation of undissolved solids from the resulting solution.
To obviate eutrophication of lakes, streams, etc. , non-phosphorus highly biodegradable builders and sequestrants are provided for household and industrial use. These builders and sequestrants are either (1) a cis-2,5-disubstituted tetrahydrofuran in which the substituents are carboxy or carboxymethyl groups, (2) water soluble salts of such tetrahydrofurans, or (3) mixtures of (1) and (2). Conventional detergent actives may also be utilized in combination with the builders or sequestrants of this invention.
Preparation Of 4-(.Alpha.-Alkyl-.Alpha.-Cyano-Methyl)-2,6-Di-Substituted Phenols
Charles R. Everly - Baton Rouge LA Gene C. Robinson - Baton Rouge LA
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07C12175 C07C 6966
US Classification:
260465F
Abstract:
4-(. alpha. -hydrocarbyl-. alpha. -cyano-methyl)2,6-di-substituted phenols having the formula ##STR1## wherein R is selected from hydrogen, hydrocarbyl radicals, substituted hydrocarbyl radicals and hydrocarbyloxy radicals and R. sub. 1 and R. sub. 2 are the same or different monovalent substituent selected from the group consisting of alkyl, aralkyl and cyclic alkyl radicals and are prepared by reacting a di-substituted phenol having the formula ##STR2## when R. sub. 1 and R. sub. 2 are as defined above with an aldehyde having at least one aldehyde radical and containing an R group as defined above and an alkali metal cyanide or an alkaline earth metal cyanide in a suitable solvent. The 4-(. alpha. -hydrocarbyl-. alpha. -cyano-methyl)2,6-di-substituted phenol thus formed can readily be converted to the corresponding 4-(. alpha.
Preparation Of Polyalkylated Cyclopentadienes From Isobornyl Carboxylates
William J. Layman - Orangeburg SC Gene C. Robinson - Baton Rouge LA
Assignee:
Albemarle Corporation - Richmond VA
International Classification:
C07C 1328 C07C 120
US Classification:
585352
Abstract:
A process for preparing tetraalkylated cyclopentadienes comprises (a) pyrolyzing an isobornyl carboxylate so as to form a mixture of 1,2,3- and 1,2,4-trimethylcyclopentadienes, (b) alkylating said mixture with an alkylating agent so as to form a mixture of alkyltrimethylcyclopentadiene isomers including 1,2,3,4-alkyltrimethylcyclopentadiene and, (c) thermally isomerizing the mixture of isomers obtained in step (b) so as to increase the proportion of 1,2,3,4-alkyltrimethylcyclopentadiene in said mixture of isomers.
Diels-Alder Type Process Involving A Geminal-Dihalocyclopropane And A Dienophile
Adducts containing a six-membered olefinically unsaturated ring having a halogen atom on one of the ethylenic carbon atoms (e. g. , 3,5-diketo-4,8-dioxa-12-chlorotricyclo[5. 3. 2. sup. 2,6 ]-dodec-11-ene) are formed by heating a dienophile (e. g. , maleic anhydride) with a gem-dihalocyclopropane which has at least 4 carbon atoms in the molecule and at least one hydrogen on a carbon atom singly bonded to the cyclopropane ring (e. g. , 7,7-dichloro-2-oxabicyclo[4. 1. 0] heptane). The adducts have toxicological properties and thus may be used as insecticides, fungicides, bactericides, herbicides, miticides and the like. They are also useful in the manufacture of plasticizers, flameproofing agents, water mark detecting agents, waterproofing agents, degreasing solvents, surface active agents, and the like.
Providence Kodiak Island Medical Center Specialty Clinic 1915 E Rezanof Dr, Kodiak, AK 99615 9074869580 (phone), 9074869586 (fax)
Education:
Medical School University of California, San Diego School of Medicine Graduated: 1982
Languages:
English Spanish Tagalog
Description:
Dr. Robinson graduated from the University of California, San Diego School of Medicine in 1982. He works in Kodiak, AK and specializes in General Surgery. Dr. Robinson is affiliated with Providence Kodiak Island Medical Center.
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