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  2. Propionaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propionaldehyde

    It is used in the synthesis of several common aroma compounds (cyclamen aldehyde, helional, lilial). [2] Reduction of propionaldehyde gives n‑propanol, and reductive amination gives propanamine. Rising demand for non-chlorocarbon solvents has caused some manufacturers to substitutively brominate n‑propanol to propyl bromide.

  3. Propiolaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propiolaldehyde

    This page was last edited on 9 September 2024, at 02:19 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  4. Phenylacetone - Wikipedia

    en.wikipedia.org/wiki/Phenylacetone

    Phenylacetone, also known as phenyl-2-propanone, is an organic compound with the chemical formula C 6 H 5 CH 2 COCH 3.It is a colorless oil that is soluble in organic solvents.It is a mono-substituted benzene derivative, consisting of an acetone attached to a phenyl group.

  5. Knoevenagel condensation - Wikipedia

    en.wikipedia.org/wiki/Knoevenagel_condensation

    The Weiss–Cook reaction consists in the synthesis of cis-bicyclo[3.3.0]octane-3,7-dione employing an acetonedicarboxylic acid ester and a diacyl (1,2 ketone). The mechanism operates in the same way as the Knoevenagel condensation: [10]

  6. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    The latter reaction is also viable laboratory synthesis. One laboratory technique for substitutive bromination treats propanol with a mixture of hydrobromic and sulfuric acids: CH 3 CH 2 CH 2 OH + HBr → CH 3 CH 2 CH 2 Br + H 2 O. Alternate synthetic routes include treating propanol with phosphorus tribromide [4] or via a Hunsdiecker reaction ...

  7. Pinacol coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Pinacol_coupling_reaction

    The pinacol reaction is extremely well-studied and tolerates many different reductants, including electrochemical syntheses.Variants are known for homo- and cross-coupling, intra- and inter-molecular reactions with appropriate diastereo- or enantioselectivity; [2] as of 2006, the only unsettled frontier was enantioselective cross-coupling of aliphatic aldehydes. [3]

  8. Cannizzaro reaction - Wikipedia

    en.wikipedia.org/wiki/Cannizzaro_reaction

    Thus, the yield of the valuable chemical is high, although the atom economy can be low. The final stage in the synthesis of pentaerythritol is an example. A solvent-free reaction has been reported involving grinding liquid 2-chlorobenzaldehyde with potassium hydroxide in a mortar and pestle: [7] Solvent-free Cannizzaro reaction

  9. Silyl enol ether - Wikipedia

    en.wikipedia.org/wiki/Silyl_enol_ether

    The general structure of a silyl enol ether. In organosilicon chemistry, silyl enol ethers are a class of organic compounds that share the common functional group R 3 Si−O−CR=CR 2, composed of an enolate (R 3 C−O−R) bonded to a silane (SiR 4) through its oxygen end and an ethene group (R 2 C=CR 2) as its carbon end.