Английская Википедия:Diethylsuccinoylsuccinate

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Версия от 08:40, 27 февраля 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{Chembox | ImageFile = Et2succinoylsuccinate.svg | ImageSize = | ImageAlt = | PIN = Diethyl 2,5-dihydroxycyclohexa-1,4-diene-1,4-dicarboxylate | OtherNames = 2,5-Dihydroxy-1,4-cyclohexadiene-1,4-dicarboxylic acid<br>1,4-Bis(ethoxycarbonyl)-2,5-dihydroxy-1,4-cyclohexadiene |Section1={{Chembox Identifiers | CASNo = 16877-79-5 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 7ST9KV5XVD |...»)
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Diethylsuccinoylsuccinate is an organic compound with the formula [CH2C(OH)=C(CO2Et)]2 (Et = ethyl). A tetrasubstituted derivative of 1,4-cyclohexadiene, the compound is the enol tautomer of the corresponding cyclohexadione.[1] It is produced by base-induced condensation of diethyl succinate:[2]

2 EtO2CCH2CH2CO2Et [CH2C(OH)=C(CO2Et)]2 + 2 EtOH

Diethylsuccinylsuccinate is valued as a precursor to the quinacridone pigments. For example, it reacts with two equiv of anilines to give the diamines [CH2C(N(H)Ar)=C(CO2Et)]2, which undergoes cyclization upon treatment with acid to give dihydroquinacridone.[3][4][5]

When heated in the presence of acid, diethylsuccinoylsuccinate converts to 1,4-cyclohexanedione via hydrolysis of the esters followed by decarboxylation.[2]

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