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  2. Diethyl succinate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_succinate

    Diethyl succinate is the diethyl ester of succinate. It is a colorless liquid with the formula (CH 2 CO 2 Et) 2 (Et = ethyl). The organic molecule contains two ester groups. This ester is a versatile chemical intermediate. A colorless liquid, diethyl succinate is formed by Fischer esterification of succinic acid and ethanol.

  3. Stobbe condensation - Wikipedia

    en.wikipedia.org/wiki/Stobbe_condensation

    Commonly, diethylsuccinate is a component of the reaction. The usual product is salt of the half-ester. The Stobbe condensation is named after its discoverer, Hans Stobbe, whose work involved the sodium ethoxide-induced condensation of acetone and diethyl succinate. [2] An example is the reaction of benzophenone with diethyl succinate: [3]

  4. Succinic acid - Wikipedia

    en.wikipedia.org/wiki/Succinic_acid

    Succinic acid (/ s ə k ˈ s ɪ n ɪ k /) is a dicarboxylic acid with the chemical formula (CH 2) 2 (CO 2 H) 2. [5] In living organisms, succinic acid takes the form of an anion, succinate, which has multiple biological roles as a metabolic intermediate being converted into fumarate by the enzyme succinate dehydrogenase in complex 2 of the electron transport chain which is involved in making ...

  5. 1,4-Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/1,4-Cyclohexanedione

    Specifically under basic conditions, the diethyl succinate condenses to give the cyclohexenediol derivative diethylsuccinoylsuccinate. This intermediate can be hydrolysed and decarboxylated to afford the desired dione. [2] This dione condenses with malononitrile to give an intermediate that can be dehydrogenated to tetracyanoquinodimethane ...

  6. C8H14O4 - Wikipedia

    en.wikipedia.org/wiki/C8H14O4

    Diethyl succinate; Dimethyl_adipate; Ethyl acetoxy butanoate; Fructone; Suberic acid; 2,2,3,3-Tetramethylsuccinic acid This page was last edited on 24 July 2022, at ...

  7. Diethyl malonate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_malonate

    Diethyl malonate, also known as DEM, is the diethyl ester of malonic acid. It occurs naturally in grapes and strawberries as a colourless liquid with an apple-like odour, and is used in perfumes. It is also used to synthesize other compounds such as barbiturates, artificial flavourings, vitamin B 1, and vitamin B 6.

  8. Diethylene glycol - Wikipedia

    en.wikipedia.org/wiki/Diethylene_glycol

    Diethylene glycol (DEG) is an organic compound with the formula (HOCH 2 CH 2) 2 O. It is a colorless, practically odorless, and hygroscopic liquid with a sweetish taste. It is a four carbon dimer of ethylene glycol.

  9. Category:Ethyl esters - Wikipedia

    en.wikipedia.org/wiki/Category:Ethyl_esters

    This page was last edited on 13 February 2024, at 22:20 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.