In re Breslow

616 F.2d 516, 205 U.S.P.Q. (BNA) 221, 1980 CCPA LEXIS 279
CourtCourt of Customs and Patent Appeals
DecidedFebruary 28, 1980
DocketAppeal No. 79-602
StatusPublished
Cited by8 cases

This text of 616 F.2d 516 (In re Breslow) 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
In re Breslow, 616 F.2d 516, 205 U.S.P.Q. (BNA) 221, 1980 CCPA LEXIS 279 (ccpa 1980).

Opinions

RICH, Judge.

This appeal is from the decision of the United States Patent and Trademark Office (PTO) Board of Appeals (board) affirming the rejections of claims 2, 3, and 8 in appellant’s application, serial No. 646,309,1 filed [517]*517January 2, 1976, for “Nitrile Imines,” under 35 U.S.C. § 101 for failure to define a statutory class of invention and also under 35 U.S.C. § 112, first paragraph, for not disclosing how to prepare and isolate the claimed compounds. We reverse.

The Invention

The new compounds claimed herein, poly-functional nitrile imines, are one aspect of a broader invention which is described in U.S. Patent No. 3,418,285, which issued on a parent application, as follows: “This invention relates to new cross-linking agents, to cross-linking unsaturated polymers therewith, and to the crosslinked products so produced.” The instant application explains that generally any type of unsaturated polymer, containing ethylenic unsaturation wherein there is at least one hydrogen radical attached to at least one of the carbon atoms of the double bond, can be cross-linked with the polyfunctional nitrile imines and that the resulting cross-linked polymers are hard, tough rubbers, substantially insoluble in water and hydrocarbon solvents with improved tensile properties useful in various rubber applications.

The following quotations from appellant’s specification are particularly relevant to the issue before us:

The polyfunctional nitrile imines of this invention are relatively unstable compounds, and the primary modes of cross-linking unsaturated polymers with these imines involves their formation in situ in a polymer mass from their closely related but more stable hydrogen chloride salts * * * usually accomplished by contacting the hydrazide chloride with an alkaline material. * * *
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The cross-linking is carried out by contacting the unsaturated polymer and a minor amount of the polyfunctional nitrile imine cross-linking agent for a time sufficient for the desired degree of cross-linking to occur. This uniform contacting is preferably achieved by uniformly mixing the polymer and the hydrogen chloride salt of the polyfunctional nitrile imine, and treating that mixture with an alkaline material, thereby generating the nitrile imine in situ in the polymer mass. ******
The uniform mixing * * * Can be carried out by milling these ingredients on a conventional rubber mill, by dissolving the hydrogen chloride salt or the tetrazole precursor in a solvent solution of the polymer, or by any of other numerous methods, which will be readily apparent to those skilled in the art. This uniform contacting will result in the nitrile imine cross-linking agent being uniformly distributed throughout the polymer mass upon its in situ generation, so that uniform cross-linking can be achieved.

Thus, the claimed compounds are simultaneously generated and put to use. The three product claims on appeal are in Markush form, covering a large number of nitrile imines, the novelty, utility, and unobviousness of which have not been questioned. In view of the nature of the rejections, it will not be necessary to consider the claims in detail and quoting them would serve no useful purpose.

The Rejection

The examiner relief on no prior art references. He held, first, that the claimed compounds do not fall within any statutory category of invention named in 35 U.S.C. § 101.2 For support, he relied on three admissions which appeared in the file of the parent application (serial No. 453,664), as follows: (1) “It is true that the compounds are transitory intermediates”; (2) “they are [518]*518so reactive that they will react with each other if there is no other coreactant available”; and (3) “it is also true that applicant has not isolated the compounds.” On the basis of these admissions, the examiner said in his Answer:

A “transitory intermediate” is not a composition of matter provided for under the normal interpretation of this statute. * * *
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* * * as noted above (and below) this is a situation where a “transitory” intermediate, which would not and could not be readily isolated, is being claimed and one of ordinary skill in the art is not presented with an enabling disclosure (for more on “enablement” see below) for attaining this compounds, [sic] per se, claimed at bar.
Decisions: While no direct precedential decisions have been found that are specifically in point on this 35 U.S.C. [§] 101 issue the following decisions might be of interest: Ex parte Howard, 1924 C.D. 75 (item No. 1 on page 76) and In re Stubbs, 1932 C.D. 466 (item No. 1 on page 467).

The examiner then made a second rejection of the appealed claims under 35 U.S.C. § 112, first paragraph, saying:

The first paragraph is pertinent as this disclosure provides no “enabling” data to teach one of ordinary skill in the art how to prepare and isolate the compounds, per se, presently being claimed. Derivatives yes, but actual isolatable compounds, no.
Put another way, it is clear that as appellant is claiming specific compounds it is appellant’s duty (to fulfill the patent contract granted by the government of the United States)3 to give sufficient teachings to enable one of ordinary skill in the art to produce (or reproduce) and isolate such claimed compounds, per se, not derivatives thereof. As urged by the Examiner, supra, appellant has not done so. If it would be obvious to the ordinary skill in the art how to isolate such claimed compounds then no problem exists as such would be patentable * * * but herein no such enablement is proffered nor is (are) any reference(s) cited to prove such isolation would be within the ordinary skill of the art. [Emphasis ours.]

Another argument made by the examiner was that there was no indication, and certainly no proof, that the claimed compounds “are even formed.” The board disagreed with him on this point and expressly held to the contrary, so that question is not before us. The board held that, on the evidence produced by appellant, it is “reasonable to assume that the claimed compounds, in fact, are formed and do exist in the system disclosed by appellant in which they are specifically and explicitly taught to be produced.” Having so held, the board’s opinion continues as follows:

But we are, nevertheless, constrained to affirm the Examiner’s rejection of the instant claims. An interesting legal question is presented by this case for which, as noted by the Examiner, no direct precedential decisions appear to exist. However, similar factual situations prevailed in Ex parte Howard, 1924 CD 75, wherein a free-falling drop or gob of molten glass which exists only while falling to the mold was claimed, and in

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Bluebook (online)
616 F.2d 516, 205 U.S.P.Q. (BNA) 221, 1980 CCPA LEXIS 279, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-breslow-ccpa-1980.