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Maleic anhydride is a classic substrate for Diels-Alder reactions. [9] It was used for work in 1928, on the reaction between maleic anhydride and 1,3-butadiene, for which Otto Paul Hermann Diels and Kurt Alder were awarded the Nobel Prize in 1950. It is through this reaction that maleic anhydride is converted to many pesticides and pharmaceuticals.
In synthetic organic chemistry it is a dienophile and used in the Diels-Alder reaction. With the invention of polyaspartic technology the material also found another use. With this technology an amine is reacted with a dialkyl maleate - usually diethyl maleate - utilizing the Michael addition reaction.
The compound is manufactured by treating 2-ethylhexanol with maleic anhydride and an esterification catalyst. It is a key intermediate raw material in the production of dioctyl sulfosuccinate (DOSS, docusate) salts, used medically as laxatives and stool softeners, and in many other applications as versatile surfactants. [2] [3] [4]
For the synthesis of tetrasodium iminodisuccinate, maleic anhydride is reacted with sodium hydroxide in water at elevated temperature. A concentrated disodium maleate solution is formed to which ammonia is added [ 4 ] at 90 to 145 °C, then excess water and ammonia is distilled off.
2,3-Dimethylmaleic anhydride is an organic compound with the formula (CH 3) 2 C 2 (CO) 2 O. [1] It is related to maleic anhydride (MA) by replacement of the two CH units with CCH 3 groups. The compound can be prepared from two eqiuvalents of MA in the presence of 2-aminopyridine followed by treatment with sulfuric acid.
After the discovery of the safener properties of naphthalic anhydride, [5] additional safeners were reported. They are associated with particular crops, such as benoxacor for maize and flurazole for sorghum. [6] Approximately 20 safeners were in use in 2023. The inventory: [7] benoxacor; BPCMS; cloquintocet; cyometrinil; cyprosulfamide ...
In another process, maleic anhydride is first opened with water or another alcohol to form maleic acid and is then reacted with DCPD where an alcohol from the maleic acid reacts across one of the double bonds of the DCPD. This product is then used to end-cap the UPR resin which yields a product with unsaturation on the end-groups.
Fumaric acid is used in the making of wheat tortillas as a food preservative and as the acid in leavening. [9] It is generally used as a substitute for tartaric acid and occasionally in place of citric acid, at a rate of 1 g of fumaric acid to every ~1.5 g of citric acid, in order to add sourness, similarly to the way malic acid is used.