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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489346Generated: October 31, 2026

Water → 3-Cyclohexene-1,2-dicarboxylic acid

https://huagongshe.com/reaction/1489346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMelamineHCID 7955—
Reactant3a,4,5,7a-Tetrahydro-2-benzofuran-1,3-dioneHCID 12726601—
Product3-Cyclohexene-1,2-dicarboxylic acidHCID 12726607—

Reaction Steps

In a beaker having an inner volume of 2 liters, 800 ml of deionized water was charged and, with stirring pieces immersed therein, was stirred and boiled on a stirrer provided with a hot plate. In this hot water, 12.6 g of melamine was thoroughly dissolved. Separately, in a beaker having an inner volume of one liter, 500 ml of deionized water was charged and, with stirring pieces immersed therein, was stirred and boiled on a stirrer provided with a hot plate. In this hot water, 15.2 g of tetrahydrophthalic anhydride was added and the resultant mixture was stirred for one hour with heating to give an aqueous solution of tetrahydrophthalic acid. This aqueous solution was added to the aqueous melamine solution mentioned above and the resultant mixture was stirred. The resultant mixed solution, when cooled with ice water, precipitates crystals. The crystals were separated by filtration and then dried in a vacuum drier. By the thermal analysis (DSC), the infrared absorption analysis and the titration with KOH performed in the same manner as in Synthesis Example 1, the crystals were confirmed to have formed a salt of melamine and tetrahydrophthalic acid at a molar ratio of 1:1. This salt will be referred to hereinafter as "melamine-THPA salt".

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677450
Source datasetuspto-grants-1997_10
ORD IDord-d1463565b57249b3aa4b635b48e80764
Source noteuspto-grants-1997_10