Robert J. Ellis - Baton Rouge LA Lawrence H. Shepherd - Baton Rouge LA Richmond M. Starrett - Baton Rouge LA
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07C13912
US Classification:
260513B
Abstract:
A process is disclosed for producing alkyl sulfonates by the addition of bisulfite ions to olefinic double bonds. In the process, ammonium, or alkali metal bisulfite and olefins having from about 8 to about 30 carbon atoms per molecule are reacted in the presence of lower alkanol having from 2 to about 4 carbon atoms, water and a reaction initiating agent.
By treating a primary or secondary alkenol having an olefinic bond in the sixth position relative to the carbon atom carrying the hydroxyl group and at least one methyl group in the fifth position relative to said carbon atom with a strong acid (e. g. , 85 percent phosphoric acid), 2,2-dialkyltetrahydropyrans are produced via a cyclization reaction. The products have desirable fragrance characteristics.
Tricyclo[4. 2. 1. sup. 2,5 ]non-7-enes wherein the 3 position is substituted by a methylol group may be made by reacting a bicyclo[2. 2. 1]hepta-2,5-diene with a 2-alkenyl magnesium compound in a 1:1 ratio to yield a molecular addition product which is then oxidized and hydrolyzed to give the 3-methylol product. These substituted tricyclo[4. 2. 1. sup. 2,5 ]non-7-enes are useful, inter alia, as intermediates for the manufacture of lubricating oil additives and various other useful products and they may be used for gas scrubbing applications and the like.
Lawrence H. Shepherd - Baton Rouge LA William J. DeWitt - Baton Rouge LA Gerhard O. Kuehnhanss - Baton Rouge LA
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07C14302 C09K 300
US Classification:
260513R
Abstract:
An ether sulfinate/sulfonate or disulfonate having the following formula: ##STR1## wherein: R is a hydrocarbon group having from about 6 to about 24 carbon atoms, Y is SO. sub. 2 M or SO. sub. 3 M, Z is hydrogen or a methyl group, and M is an alkali metal, alkylammonium or ammonium cation and mixtures of each of said sulfinate/sulfonate and said disulfonate with an ether monosulfonate having the following formula: ROCH. sub. 2 CH(Z)CH. sub. 2 SO. sub. 3 M wherein: R is a hydrocarbon group having from about 6 to about 24 carbon atoms, Z is hydrogen or a methyl group, and M is an alkali metal, alkylammonium or ammonium cation.
John Y. Lee - Baton Rouge LA Lawrence H. Shepherd - Baton Rouge LA
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07C 8524
US Classification:
564412
Abstract:
A process of selectively preparing p-bromo-o-alkylanilines (e. g. 4-bromo-2-methylaniline) by reacting o-alkylanilines (e. g. , 2-methylaniline) with unadsorbed bromine in a solvent selected from the group consisting of an inert di- tri- or tetrahaloaliphatic hydrocarbon (e. g. , dichloromethane and dibromomethane), an alkyl nitrile (e. g. , acetonitrile) and mixtures thereof.
Kevin J. Theriot - Baton Rouge LA Niomi L. Krzystowczyk - Baton Rouge LA Edward A. Burt - Baton Rouge LA Lawrence H. Shepherd - Baton Rouge LA
Assignee:
Albemarle Corporation - Richmond VA
International Classification:
C07C 1724 C07C 1733 C07C 2513 C07C 2502
US Classification:
570142
Abstract:
Activated carboxylic acids and esters such as pentafluorobenzoic acid are rapidly decarboxylated in high yields by reacting the acid or ester with an alkanolamine reagent which catalyzes the reaction.
Aldehydes are produced by cleaving 2,2-dialkyltetrahydropyrans bearing two hydrogen atoms in the sixth position with a strong acid. The 2,2-dialkyltetrahydropyran can be formed in situ by contacting the strong acid with a primary 6-alken-1-ol having at least one methyl group in the fifth position so that cyclization occurs.
Process For Converting Exo-Isomers Of Alkyl Substituted Cyclopentadienes To Endo-Isomers