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  2. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    1-Bromobutane is the precursor to n-butyllithium: [4] 2 Li + C 4 H 9 X → C 4 H 9 Li + LiX where X = Cl, Br. The lithium for this reaction contains 1-3% sodium. When bromobutane is the precursor, the product is a homogeneous solution, consisting of a mixed cluster containing both LiBr and LiBu.

  3. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    1-Bromobutane; 2-Bromobutane; Except ... or via a Hunsdiecker reaction with butyric acid. [5 ... It is an aggressive solvent with a Kauri-butanol value of 129 which ...

  4. n-Butyllithium - Wikipedia

    en.wikipedia.org/wiki/N-Butyllithium

    The standard preparation for n-BuLi is reaction of 1-bromobutane or 1-chlorobutane with Li metal: [3] 2 Li + C 4 H 9 X → C 4 H 9 Li + LiX (X = Cl, Br) If the lithium used for this reaction contains 1–3% sodium, the reaction proceeds more quickly than if pure lithium is used.

  5. 1-Butanol - Wikipedia

    en.wikipedia.org/wiki/1-Butanol

    1-Butanol, also known as butan-1-ol or n-butanol, is a primary alcohol with the chemical formula C 4 H 9 OH and a linear structure. Isomers of 1-butanol are isobutanol, butan-2-ol and tert-butanol. The unmodified term butanol usually refers to the straight chain isomer.

  6. Butyl iodide - Wikipedia

    en.wikipedia.org/wiki/Butyl_iodide

    184.020 g·mol −1 Appearance Colourless liquid Density: 1.617 g mL −1: ... 1-Bromobutane; 1-Chlorobutane; 1-Fluorobutane; References This page was last edited on ...

  7. Butanol - Wikipedia

    en.wikipedia.org/wiki/Butanol

    Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 O H, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuOH, and t-BuOH).

  8. Tetrabutylammonium bromide - Wikipedia

    en.wikipedia.org/wiki/Tetrabutylammonium_bromide

    Tetrabutylammonium bromide can be prepared by the alkylation of tributylamine with 1-bromobutane. [2] Tetrabutylammonium bromide is used to prepare other salts of the tetrabutylammonium cation by salt metathesis reactions. [7] It serves as a source of bromide ions for substitution reactions.

  9. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide used to study the massive deadenylation of adenine based-nucleosides induced by halogenated alkanes (alkyl halides) under physiological conditions. 2-Bromo-2-methylpropane causes the massive deguanylation of guanine based-nucleosides and massive deadenylation of adenine based-nucleosides.