ROSENQUIST v. SCHOLL et al - Page 4




               Patent Interference No. 103,812                                                                                     

               party Rosenquist has demonstrated an actual reduction to practice of an invention within the                        
               scope of count 2 prior to May 20, 1994, the effective filing date of Scholl's involved Application                  
               08/438,516.  Jepson v. Egly, 231 F.2d 947, 957, 109 USPQ 354, 362 (CCPA 1956); see also                             
               Price v. Symsek, 988 F.2d 1187, 1190, 26 USPQ2d 1031, 1033 (Fed. Cir. 1993).  Rosenquist                            
               focuses his priority case on Rosenquist patent claim 1.  See RB, p. 12.  Therefore, we also focus                   
               our attention on Rosenquist patent claim 1.                                                                         
                       Rosenquist patent claim 1 is directed to a process for preparing a high molecular weight                    
               compound having a molecular weight of at least 1,125.  The compound comprises (a) a                                 
               condensation product comprising (i) a bis-phenol derivative and (ii) a phosgene derivative or a                     
               carbonate ester and (b) an endcapping or chain stopping molecule, including 3-(2H-benzotriazol-                     
               2-yl)-5-(1,1-dimethylethyl)-4-hydroxy-benzene-propanoic acid, wherein the endcapping agent is                       
               chemically bound to the condensation product by an ester linkage.4  The process comprises (a)                       
               interfacially condensing a phosgene derivative, a bis-phenol derivative and an endcapping or                        
               chain stopping molecule, including 3-(2H-benzotriazol-2-yl)-5-(1,1-dimethylethyl)-4-hydroxy-                        
               benzene-propanoic acid, wherein the endcapping agent is chemically bound to the condensation                        
               product by an ester linkage through the acid substituent of the phenolic substituent of the                         
               endcapping or chain stopping molecule and (b) adding a base.                                                        



                       4The structural formula of 3-(2H-benzotriazol-2-yl)-5-(1,1-dimethylethyl)-4-hydroxy-                        
               benzene-propanoic acid is said to correspond to the first of the two endcapping or chain stopping                   
               molecules recited in Rosenquist patent claim 1 wherein R1 is a four carbon atom alkyl group, R2                     
               is hydrogen and n is 2.  See RR, pp. 3-4, paragraph 6.                                                              

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