US2004152592A1PendingUtilityA1

Process for producing carbonyl or hydroxy compound

Assignee: SUMITOMO CHEMICAL COMPANY LIMTPriority: Aug 11, 2000Filed: Jan 21, 2004Published: Aug 5, 2004
Est. expiryAug 11, 2020(expired)· nominal 20-yr term from priority
C07C 45/294C07C 45/28B01J 21/02C07C 49/258C07C 29/03C07C 409/14C07C 409/04B01J 23/28C07C 67/31B01J 23/30C07C 407/00C07C 2601/02C07C 45/53C07C 2602/20C07C 67/333C07B 41/00C07C 51/31C07C 51/16
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Claims

Abstract

There are disclosed are a method for producing at least one compound selected from a carbonyl compound and a hydroxy adduct compound by an oxidative cleavage or addition reaction of an olefinic double bond of an olefin compound, which contains reacting an olefin compound with hydrogen peroxide, utilizing as a catalyst, at least one member selected from (a) tungsten, (b) molybdenum, or (c) a tungsten or molybdenum metal compound containing (ia) tungsten or (ib) molybdenum and (ii) an element of Group IIIb, IVb, Vb or VIb excluding oxygen, and a catalyst composition.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . An oxidation catalyst composition obtained by reacting aqueous hydrogen peroxide with at least one member selected from 
 (a) a tungsten or molybdenum metal compound comprising 
 (ia) tungsten or (ib) molybdenum and  
 (ii) an element of Group IIIb, IVb, Vb or VIb excluding oxygen, provided that said tungsten metal compound is not tungstencarbide.  
   
     
     
         2 . An oxidation catalyst composition obtained by reacting aqueous hydrogen peroxide with at least one member selected from 
 (a) tungsten,    (b) molybdenum, or    (c) a tungsten or molybdenum metal compound comprising 
 (ia) tungsten or (ib) molybdenum, and  
 (ii) an element of Group IIIb, IVb, Vb or VIb excluding oxygen, and containing an organic solvent.  
   
     
     
         3 . The oxidation catalyst according to  claim 1  or  2 , wherein the metal compound is tungsten boride, tungsten disulfide or molybdenum boride.  
     
     
         4 . The oxidation catalyst according to  claim 2 , wherein the organic solvent is t-butanol or methyl t-butyl ether.  
     
     
         5 . The oxidation catalyst according to  claim 4 , which is dehydrated.  
     
     
         6 . The oxidation catalyst according to  claim 5 , wherein dehydrating is conducted by using anhydrous magnesium sulfate.

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