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  2. Claisen condensation - Wikipedia

    en.wikipedia.org/wiki/Claisen_condensation

    claisen-condensation. RSC ontology ID. RXNO:0000043. The Claisen condensation is a carbon–carbon bond forming reaction that occurs between two esters or one ester and another carbonyl compound in the presence of a strong base. The reaction produces a β-keto ester or a β- diketone. [1] It is named after Rainer Ludwig Claisen, who first ...

  3. Alkoxide - Wikipedia

    en.wikipedia.org/wiki/Alkoxide

    The structure of the methoxide ion. In chemistry, an alkoxide is the conjugate base of an alcohol and therefore consists of an organic group bonded to a negatively charged oxygen atom. They are written as RO−, where R is the organyl substituent. Alkoxides are strong bases [citation needed] and, when R is not bulky, good nucleophiles and good ...

  4. Darzens reaction - Wikipedia

    en.wikipedia.org/wiki/Darzens_reaction

    The Darzens reaction (also known as the Darzens condensation or glycidic ester condensation) is the chemical reaction of a ketone or aldehyde with an α-haloester in the presence of a base to form an α,β- epoxy ester, also called a "glycidic ester". [1][2][3] This reaction was discovered by the organic chemist Auguste Georges Darzens in 1904 ...

  5. Sodium methoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_methoxide

    Sodium methoxide is prepared by treating methanol with sodium: 2 Na + 2 CH 3 OH → 2 CH 3 ONa + H 2. The reaction is so exothermic that ignition is possible. The resulting solution, which is colorless, is often used as a source of sodium methoxide, but the pure material can be isolated by evaporation followed by heating to remove residual methanol.

  6. Sodium ethoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_ethoxide

    Sodium ethoxide is commonly used as a base in the Claisen condensation [7] and malonic ester synthesis. [8] Sodium ethoxide may either deprotonate the α-position of an ester molecule, forming an enolate, or the ester molecule may undergo a nucleophilic substitution called transesterification. If the starting material is an ethyl ester, trans ...

  7. Tishchenko reaction - Wikipedia

    en.wikipedia.org/wiki/Tishchenko_reaction

    tishchenko-reaction. The Tishchenko reaction is an organic chemical reaction that involves disproportionation of an aldehyde in the presence of an alkoxide. The reaction is named after Russian organic chemist Vyacheslav Tishchenko, who discovered that aluminium alkoxides are effective catalysts for the reaction. [ 1 ][ 2 ][ 3 ] In the related ...

  8. Sol–gel process - Wikipedia

    en.wikipedia.org/wiki/Sol–gel_process

    The sol–gel process is a wet-chemical technique used for the fabrication of both glassy and ceramic materials. In this process, the sol (or solution) evolves gradually towards the formation of a gel-like network containing both a liquid phase and a solid phase. Typical precursors are metal alkoxides and metal chlorides, which undergo ...

  9. Ester - Wikipedia

    en.wikipedia.org/wiki/Ester

    In the Claisen condensation, an enolate of one ester (1) will attack the carbonyl group of another ester (2) to give tetrahedral intermediate 3. The intermediate collapses, forcing out an alkoxide (R'O −) and producing β-keto ester 4. The Claisen condensation involves the reaction of an ester enolate and an ester to form a beta-keto ester.