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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398033Generated: October 25, 2026

Adipic Acid → Adipic Acid

https://huagongshe.com/reaction/2398033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAdipic AcidHCID 196—
Reactant1,4-CyclohexanedimethanamineHCID 17354—
Reactant[1-(Aminomethyl)cyclohexyl]methanamineHCID 71994—
ReactantHCID 178511245HCID 178511245—
ProductAdipic AcidHCID 196—
ProductHexamethylenediamineHCID 16402—

Reaction Steps

Polyamides derived from cyclohexanebis (methylamine) are known in the prior art. In U.S. Pat. No. 3,012,994 polyamides derived from the condensation of 1,3- or 1,4-cyclohexanebis(methylamine) and a dicarboxylic acid are described. These polyamides possess good stability and strength properties and are described as having relatively high melting points; for example, the polyamide of trans-1, 4cyclohexane-bis(methylamine) and adipic acid has a crystalline melting point of 345° C., whereas nylon 66 formed from hexamethylene diamine and adipic acid has a melting point of only 264° C. However, the high melting point advantage of these polyamides also gives rise to certain inherent disadvantages. For example, polyamides having crystalline melting points much above about 300° C. tend to decompose into degradation products prior to melting. As a result filaments formed from these high melting polyamides generally have poor processability and inferior properties. Although lower melting polyamides can be obtained with trans-1,4cyclohexanebis(methylamine) by condensation with longer chain carboxylic acids, the use of the longer chain acids results in a decrease in the dimensional stability of the resulting polyamide. An object of the present invention is to provide polyamides derived from components comprising a cyclohexanebis(alkylamine) which have good dimensional stability and which have substantially lower melting points than the corresponding polyamides derived from cyclohexanebis(methylamine).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04024114
Source datasetuspto-grants-1977_05
ORD IDord-63ca0a3e22004274b8c82bd15d82b4c5
Source noteuspto-grants-1977_05