Application of John R. Stemniski

444 F.2d 581, 58 C.C.P.A. 1410
CourtCourt of Customs and Patent Appeals
DecidedOctober 7, 1971
DocketPatent Appeal 8434
StatusPublished
Cited by27 cases

This text of 444 F.2d 581 (Application of John R. Stemniski) is published on Counsel Stack Legal Research, covering Court of Customs and Patent Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Application of John R. Stemniski, 444 F.2d 581, 58 C.C.P.A. 1410 (ccpa 1971).

Opinion

BALDWIN, Judge.

This appeal is from the decision of the Patent Office Board of Appeals affirming the examiner’s rejection of claims 10-12 1 under 35 U.S.C. § 103 as obvious in view of certain prior art. We reverse.

The Invention

The invention relates to monomeric divalent, or polymeric disubstituted, ór-gano tin compounds of the formula appearing and defined in representative claim 10:

10. A disubstituted tin compound of the formula [Ri-Sn-R2]a wherein each of Ri and R2 is a substituent selected from the class consisting of aryl-oxyaryl radicals containing from 2 to *582 3 benzene rings, wherein each said aryl radical is an aromatic hydrocarbon radical, and n is an integer with a value of at least one.

Claims 11 and 12 are directed to monomeric and polymeric bis (phenoxy-phenyl) tin, respectively, wherein each of Ri and R2 appearing in claim 10 has the structure As set forth in the specification, the claimed compounds find use as high-temperature antioxidants in polyphenyl ether hydraulic, heat exchange and lubricant fluids.

Also disclosed, but not now claimed for reasons which will become apparent, are various other diaryl tin compounds, where Ri and R2 in the above formula each may be, for example, biphenylyl, phenanthryl, or naphthyl. The use recited is the same as that for the bis (aryloxyaryl) tin compounds.

The Rejection

The examiner rejected all claims under § 103 holding that the claimed subject matter would have been obvious in view of the disclosure in any of three pri- or literature references authored by Krause, 2 Bahr, 3 and Ingham 4 considered with that of a United States patent to Ramsden. 5

All the primary references disclose various diaryl tin compounds. Bahr, for example, describes the preparation of di9-phenanthryl tin and observes that its chemical behavior “corresponds to that of other diaryl tins,” e. g., it reduces silver nitrate and polymerizes as “in all diaryl tins previously known.” Similarly, Krause discloses the preparation of di-naphthyl tin and its ability to reduce silver nitrate. Ingham, perhaps the most pertinent reference, appears to be a review article which describes the state of the art in organotin compounds as of 1960. On page 517, the authors report di-2-biphenylyl tin to be a known compound of tin wherein the valence of the tin atom is 2. In general, the authors state, organotin compounds containing two organo groups “are usually polymeric substances,” although, in a few cases, monomers are obtained “which slowly polymerize on standing.”

Finally, Ramsden, the secondary reference, discloses tetravalent, preferably tetra-aryl substituted tin compounds in which the aryl groups each comprise one to three rings. As alternative aryl sub-stituents, Ramsden fairly discloses, among many others, (biphenylyl) and (phenoxy-phenyl). Ramsden mentions moth proofing and stabilization of polyvinyl chloride as alternative uses for the tetravalent compounds disclosed.

In its initial opinion, the board, like the examiner, considered Ramsden to suggest that a biphenylyl substituent may be replaced by a phenoxyphenyl group in not only tetravalent aryl-substi-tuted tin compounds but also in divalent aryl-substituted tin compounds. It stated:

* * * That the tin compound [of Ramsden] is a tetravalent tin compound is not significant as to the teaching to the chemist of the equivalence of such substituent groups. Appellant is in poor position to urge, and has not demonstrated, any patentable distinction between the now claimed phenoxylphenyl tin compounds as compared with the analogous phenyl substituted phenyl tin compounds of the primary references, in view of the acceptance of such expected equivalence in the original specification * * * [Emphasis supplied.]

The board concluded that the claimed subject matter “is clearly rendered ob *583 vious to one skilled in this art by the combined disclosures” of the references, particularly in the absence “of a proper showing to negate the structural obviousness raised by the reference combination.”

On reconsideration, it added:

* * * the substitution of a phenoxy-phenyl substituent for a phenyl-phenyl substituent in a tin compound is in our opinion rendered obvious to the chemist by the Ramsden disclosure of the alternative and apparently equivalent use of the two different substituted phenyl groups for the same purpose in a similar although admittedly different tin compound. [Emphasis supplied.]

Opinion

In the Patent Office view, the reference combination is sufficient to establish a prima facie ease of obviousness of appellant’s compounds. The stance of the Patent Office seems to have been predicated on the view that the claimed compounds possess a structure sufficiently closely related or analogous to the structure of the Ingham, Bahr or Krause compounds (though not isomers or homo-logs of the reference compounds in the classic sense) that one of ordinary skill in the art would assume that the significant properties or uses of the two sets of compounds would be substantially the same, whatever those properties or uses might be. 6

As summarized in the solicitor’s brief:

* * * Where the claimed and prior art compounds are structurally closely related, similar properties would be expected, and it is of no consequence that the property relied on is not suggested in the prior act — particularly where there is no evidence of a difference in the property and appellant’s application generally indicates as similarity in that regard.

The crux of the Patent Office position seems to be, in other words, that where a prima facie case of obviousness of claimed compounds has been established by reason of close structural similarity to prior art compounds, and that case has not been rebutted by any evidence of unexpected or unobvious properties inhering in those novel compounds which do not actually or in fact inhere in the structurally related compounds of the principal prior art references, the rejection is proper under § 103, even though those in the art at the time appellant’s invention was made may be unaware of any significant properties or uses possessed by the prior art compounds. There is arguable precedent for the Patent Office position. See In re Henze, 181 F.2d 196, 37 CCPA 1009 (1950), discussion relating .to adjacent homologs which is quoted infra); and particularly In re Riden, 318 F.2d 761

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444 F.2d 581, 58 C.C.P.A. 1410, Counsel Stack Legal Research, https://law.counselstack.com/opinion/application-of-john-r-stemniski-ccpa-1971.