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  2. 2,4-Dihydroxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2,4-Dihydroxybenzaldehyde

    2,4-Dihydroxybenzaldehyde or β-resorcylaldehyde is a phenolic aldehyde, a chemical compound with the formula C 7 H 6 O 3. It is an isomer of protocatechuic aldehyde (3,4-dihydroxybenzaldehyde). References

  3. 2,4-Dihydroxybenzoic acid - Wikipedia

    en.wikipedia.org/wiki/2,4-Dihydroxybenzoic_acid

    2,4-Dihydroxybenzoic acid (β-resorcylic acid) is a dihydroxybenzoic acid. As a resorcylic acid, it is one of the three isomeric crystalline acids that are both carboxyl derivatives of resorcinol and dihydroxy derivatives of benzoic acid. [4] Synthesis from resorcinol is via the Kolbe-Schmitt reaction. [5]

  4. Pomeranz–Fritsch reaction - Wikipedia

    en.wikipedia.org/wiki/Pomeranz–Fritsch_reaction

    A possible mechanism is depicted below: [5] proposed mechanism Pomeranz-Fritsch reaction. First the benzalaminoacetal 1 is built by the condensation of benzaldehyde and a 2,2-dialkoxyethylamine. After the condensation a hydrogen-atom is added to one of the alkoxy groups. Subsequently, an alcohol is removed. Next, the compound 2 is built. After ...

  5. Dihydroxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzaldehyde

    Dihydroxybenzaldehyde may refer to: 2,4-Dihydroxybenzaldehyde; 3,4-Dihydroxybenzaldehyde This page was last edited on 26 November 2024, at 04:05 (UTC). Text is ...

  6. Shapiro reaction - Wikipedia

    en.wikipedia.org/wiki/Shapiro_reaction

    Addition of water (c) results in 2-bornene (4) and addition of an alkyl bromide (d) gives 5 Importantly, the Shapiro reaction cannot be used to synthesize 1-lithioalkenes (and the resulting functionalized derivatives), as sulfonylhydrazones derived from aldehydes undergo exclusive addition of the organolithium base to the carbon of the C–N ...

  7. Piperonal - Wikipedia

    en.wikipedia.org/wiki/Piperonal

    Piperonal can be prepared by the oxidative cleavage of isosafrole or by using a multistep sequence from catechol or 1,2-methylenedioxybenzene.Synthesis from the latter chemical is accomplished through a condensation reaction with glyoxylic acid followed by cleaving the resulting α-hydroxy acid with an oxidizing agent.

  8. Sommelet reaction - Wikipedia

    en.wikipedia.org/wiki/Sommelet_reaction

    The Sommelet reaction is an organic reaction in which a benzyl halide is converted to an aldehyde by action of hexamine and water. [1] [2] It is named after the French chemist Marcel Sommelet, who first reported the reaction in 1913. [3] One example, thiophene-2-carboxaldehyde is prepared by the reaction of hexamine with 2-chloromethylthiophene ...

  9. C7H6O3 - Wikipedia

    en.wikipedia.org/wiki/C7H6O3

    2,4-Dihydroxybenzaldehyde; 3,4-Dihydroxybenzaldehyde; Monohydroxybenzoic acids. ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; ...