Ex parte YAMAMOTO et al. - Page 5




              Appeal No. 96-2322                                                                           5                
              Application No. 08/112,478                                                                                    

              required by the claimed subject matter.  Furthermore, there is no disclosure in Yamazaki                      

              of “directly drying the reaction product.”  The reference, in contrast, specifically                          

              discloses a process step of filtering the oxamide to obtain the final product.  See                           

              Operational Examples 1 through 9, pages 7 and 8.  Although the examiner states that,                          

              “[g]etting product by wet solid or by filtering is certainly a physical phenomena which                       

              one of ordinary skill in the art can optimize by routine experimentation,” Answer, page                       

              6, in our view that conclusion depends upon the evidence present on the record before                         

              us with respect to that limitation.  The only suggestion for direct drying and the                            

              consequent omission of the filtration step comes solely from appellants’ specification.                       

              Accordingly, we conclude that there is no basis for the examiner’s conclusion that                            

              obtaining a wet solid or filtering the product are equivalent procedural steps.                               

              Since Yamazaki fails to disclose a limited amount of alcohol, the examiner relies                             

              upon Nemec to disclose an analogous process which is both continuous and is performed                         

              in the absence of alcohol.  Nemec’s process however, specifically excludes oxalic acid                        

              ester from the diesters disclosed therein. We find that Nemec requires that the number                        

              of carbon groups between two carboxylic acid amide groups must be at least two.  See                          

              column 1, lines 13-28.  In addition, as Nemec uses an ethylene glycol diester of an                           

              aliphatic dicarboxylic acid, the by-product obtained from the formation of amide is                           

              ethylene glycol as opposed to the aliphatic alcohol of the claimed subject matter.  We                        

              further find that filtering and/or other purification steps of the product is uniformly                       






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