Ex Parte RICHTER et al - Page 10


               Appeal No. 1999-1008                                                                                                   
               Application 08/713,905                                                                                                 

               specified in Example 1” was phosgenated in liquid phase in monochlorobenzene solvent by a                              
               process that was not attributed to any prior art reference (cf. id., lines 27-29).  The “reaction                      
               mixture” was described thusly:                                                                                         
                    It was not possible to achieve a complete elucidation of the reaction mixture. After                              
                    blowing off of the excess phosgene with nitrogen, filtration and working up by                                    
                    distillation, 19.5 g (19.6% of the theoretical yield) of a slightly colored liquid was                            
                    obtained, having a boiling range of 80 to 85°C/).07 mbar and an NCO content in                                    
                    accordance with DIN 53 185 of 45.2%. [Id., lines 15-21.]                                                          
               It is further disclosed that modifications in solvent and in starting material did not increase “the                   
               yield of diisocyanate substantially” and that “[t]he residual chlorine content of the product was in                   
               no case below 0.1%” (id., lines 22-26).                                                                                
                       In comparison, in specification Example 1, the reaction mixture is subjected to a number                       
               different processes in working up the product mixture to a purity of 99.7% and a content of                            
               hydrolyzable chlorine of 43 ppm (page 7, line 25, to page 8, line 29, particularly page 8, lines 16-                   
               24).  We further note that appellants disclose in the specification that “[t]he process of the                         
               present invention may be carried out using known techniques,” including several disclosed in the                       
               patent literature (page 4, lines 23-25), and that recovered ether isocyanate product can “be                           
               isolated in pure form by known processes such as distillation, crystallization, extraction or film                     
               distillation, or recovered as raw product (solution)” (page 5, lines 16-21).                                           
                       Based on our review, we find that the written description in the specification in its                          
               entirety does not convey with reasonable clarity to one skilled in this art that appellants were in                    
               possession of the claimed ether diisocyanate products “having a hydrolyzable chlorine content of                       
               less than 0.1%” encompassed by appealed claim 3, when the application was filed.  Indeed, while                        
               appellants indicate that unspecified “[c]ertain ether isocyanates” produced by an unspecified                          
               prior art base phosgenation process have “residual chlorine contents (0.1%),” that is, 1000 ppm,                       
               which is “very high” and not useful as “raw materials for coating,” they have also described at                        
               least one specific prior art process as producing ether (poly)isocyanates at a hydrolyzable                            
               chlorine content as low as 400 ppm, which content is further described to be “far too high for                         
               many applications, particularly . . . coating compositions.”  Not only does the latter disclosure                      
               beg the question of what is an acceptable chlorine content for an ether isocyanate in ppm for                          
               coating compositions to one skilled in this art if 400 ppm is far too high for that purpose, but it                    

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