Ex parte JAFFE et al. - Page 3




          Appeal No. 96-0700                                                          
          Application No. 08/153,550                                                  


               There is no dispute that Christmann discloses a process for            
          preparing a yellow pigment which is analogous to the claimed                
          process, i.e., Christmann utilizes tetrabromophthalic anhydride             
          as a reactant instead of the claimed tetrachlorophthalic                    
          anhydride.  We note "[a]ppellants agree that the process of                 
          present claim 1 is analogous to the reaction disclosed in the               
          Christmann et al. reference" (page 4 of Brief).  As with the                
          claimed reaction, the Christmann reaction is performed in the               
          presence of acetic acid as a solvent.  Accordingly, based upon              
          the close similarity in chemical structure between the                      
          chlorinated starting reactant of the claimed process and the                
          brominated starting material of the Christmann process, i.e., the           
          bromine substituent is the next adjacent element to chlorine in             
          the Group VIIA halogens, we concur with the examiner that it                
          would have been prima facie obvious for one of ordinary skill in            
          the art to replace the bromine substituents of Christmann with              
          the chlorine substituents of appellants with the reasonable                 
          expectation that a useful pigment would be the resultant product.           
          Moreover, we find that the conclusion of obviousness is                     
          substantially fortified by the disclosure of Hein which expressly           
          exemplifies the claimed reaction of tetrachlorophthalic anhydride           
          with o-phenphenylene diamine, albeit in a different acidic                  
          solvent.  In our view, not only would Hein strongly suggest                 
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