In re Magat

240 F.2d 351, 44 C.C.P.A. 735, 112 U.S.P.Q. (BNA) 317, 1957 CCPA LEXIS 226
CourtCourt of Customs and Patent Appeals
DecidedJanuary 9, 1957
DocketNo. 6217
StatusPublished
Cited by2 cases

This text of 240 F.2d 351 (In re Magat) 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 Magat, 240 F.2d 351, 44 C.C.P.A. 735, 112 U.S.P.Q. (BNA) 317, 1957 CCPA LEXIS 226 (ccpa 1957).

Opinion

Worley, Judge,

delivered tbe opinion of the court:

This is an appeal from the decision of the Board of Appeals of the United States Patent Office affirming the rejection by the Primary Examiner of claims 1 to 8, inclusive, of appellant’s application for a patent on a process of preparing polyamides, on the ground of lack of invention over the prior art. Claim 1 is representative' of the appealed claims and reads:

1. A process for preparing a polyamide which comprises bringing together an organic diamine in one liquid phase and an organic dicarboxylic acid halide in a second liquid phase immiscible with the first phase, mixing the liquid phases to form a system comprised of two liquid phases such that the diamine and acid halide are in separate phases and at least one of the phases includes a liquid diluent, and maintaining the phases in admixture until an interphase condensation polymerization has taken place with formation of a spinnable polyamide.

The following references were relied on by the board:

[737]*737I. G. Farbenindustrie (Fr.) 892,361 January 7, 1944. Bayer-Angewandte Cbemie September 1947, pages 257-260. De Bell et al, German Plastics, Practice, 1948, pages 283, 284, 289 and 290.

Appellant’s application relates to a method of producing a spinnable polyamide of the class commonly known as nylon which consists essentially in bringing together an organic diamine in one liquid phase and an organic dicarboxylic acid halide in a second liquid phase immiscible with the first, to form a two phase system, and maintaining them under such conditions that an interphase condensation polymerization takes place, with formation of a spinnable polyamide.

The I. G. F. French patent discloses processes for preparing poly-methanes of high molecular weight by a reaction betewen a diamine and a dichlorocarbonate derivative of a dihydroxy alcohol. The seventh example given in the patent comprises the bringing together of a solution of bis-chloro-carbonate of 1.4 butane diol in benzene and an aqueous solution of 1.6 hexamethylene diamine, to which sodium hydroxide is added, with rapid agitation. As pointed out by the board, this procedure involves the use of two liquid phases, with each of the reactants dissolved in one phase but not the other.

We are in agreement with the Patent Office tribunals that the manipulative steps set forth in the appealed claims are disclosed in all material respects by the French patent. The issue to be determined, therefore, is whether the substances disclosed by that patent are so related to those recited in the claims that the idea of applying the procedure of the patent to the latter substances would have been obvious to a person skilled in the art at the time when appellant’s alleged invention was made.

The reactants and products of the reference and the application are correctly set forth in appellant’s brief in simplified comparative form as follows:

Ref erence:
A (Diamine) + (Biscbloroformate) -> AB (Polyurethane)
Invention:
A (Diamine) -» (Dicarboxylic acid chloride) -)- A O (Polyamide)

From the above, it will be seen that while the application and reference both employ a diamine as one reactant, the second reactant and the final product differ. There appears to be a substantial difference of opinion as to just what degree of similarity exists between the second reactants and the final products in the two cases.

The examiner was of the opinion that polyurethane is a polyamide of the kind recited in the appealed claims, and that the term “organic dicarboxylic acid halide,” which appears in each of the claims, is [738]*738broad enough to include the dichloro-carbonate of a diol (also referred to in the record as bis-chloro-carbonate and bis-chloroformate) disclosed in the French patent. The board disagreed with the examiner on both points and added that “we are accordingly of the opinion that the claims should not be read as anticipated by the French patent alone.” However, the board did agree with the examiner that the claims do not define invention over what is disclosed in the French patent, concluding that “It is, however, our opinion that obvious chemical similarities and the De Bell et al citation, to which may be added the Bayer publication relied on by appellant, establish an analogy and similarity between the polyurethanes of the French patent and the polyamides here contemplated.” The board did not point out the “obvious chemical similarities” and did not explain the pertinence of the De Bell and Bayer citations.

While similarity between two products may be a factor in determining whether it would be obvious to a person skilled in the art that they could be made by similar processes, it is by no means conclusive.

The claims here are directed to processes and in such a case, as was said in In re Swain et al., 33 C. C. P. A. (Patents) 833, 154 F. 2d 118, 69 USPQ 72, “the steps comprising the process are the essential features for consideration in determining the right of appellants to a patent — not the particular material to which the process is applied nor the particular substance obtained by its application.” (Italics quoted)

Whether it would be obvious that a process of making polyurethanes could be adapted to the production of nylon-type polyamides depends primarily on the relationship between the processes by which those compounds were formerly produced. If it was common, before the invention disclosed by the French patent, to produce polyurethanes and nylon-type polyamides by the same or closely parallel processes, then it might reasonably be expected to occur to a skilled worker in the art that a process of making polyurethanes could well be modified to produce nylon-type polyamides. On the other hand, if those compounds had been produced by entirely distinct processes, there would seem to be no reason why the discoyery of a method of producing compounds of one class should suggest an attempt to produce those of the other class by similar methods.

As to the conventional method of preparing polyurethanes, it is stated in the board’s decision that “The polyurethanes are ordinarily formed from a diisocyanate and a dihydroxy compound such as butane diol. This is apparent from the He Bell et al citation.” That statement is supported by the record and appears to be correct. On the [739]*739other band, the board states that nylon-type polyamides “are ordinarily produced by condensation of a diamine, such as hexamethylene diamine (having the anine groups at the two ends of the 6 carbon atom chain) with a dicarboxylic acid such as adipic acid or a derivative thereof.” That statement also appears to be in accordance with the record.

As to the manipulative steps involved, Bayer states that in producing polyurethanes, “In contrast with the case of polyamides we can work in open vessels, for the admission of atmospheric oxygen does not cause any brown coloration of the molten polyurethane,” and that “Because of its ‘gentle’ method of preparation, perlón U is more uniform in polymerization than nylon and polycaprolactam.

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Cite This Page — Counsel Stack

Bluebook (online)
240 F.2d 351, 44 C.C.P.A. 735, 112 U.S.P.Q. (BNA) 317, 1957 CCPA LEXIS 226, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-magat-ccpa-1957.