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  2. Phosphorus tribromide - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_tribromide

    Phosphorus tribromide, like PCl 3 and PF 3, has both properties of a Lewis base and a Lewis acid. For example, with a Lewis acid such as boron tribromide it forms stable 1 :1 adducts such as Br 3 B · PBr 3. At the same time PBr 3 can react as an electrophile or Lewis acid in many of its reactions, for example with amines.

  3. Phosphorus halide - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_halide

    Phosphorus tribromide is used in organic chemistry to convert alcohols to alkyl bromides and carboxylic acids to acyl bromides (e.g. in the Hell-Volhard-Zelinsky reaction). Phosphorus triiodide also finds use in organic chemistry, as a mild oxygen acceptor.

  4. Electrophilic halogenation - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_halogenation

    However, if a catalyst is used with excess bromine, then a tribromide will be formed. Halogenation of phenols is faster in polar solvents in a basic environment due to the dissociation of phenol, with phenoxide ions being more susceptible to electrophilic attack as they are more electron-rich.

  5. Vilsmeier–Haack reaction - Wikipedia

    en.wikipedia.org/wiki/Vilsmeier–Haack_reaction

    The Vilsmeier–Haack reaction (also called the Vilsmeier reaction) is the chemical reaction of a substituted formamide (1) with phosphorus oxychloride and an electron-rich arene (3) to produce an aryl aldehyde or ketone (5):

  6. Phosphoryl bromide - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_bromide

    Phosphoryl bromide is prepared by the reaction between phosphorus pentabromide and phosphorus pentoxide: [4] [5]. 3 PBr 5 + P 2 O 5 → 5 POBr 3. It can also be prepared via the slow addition of liquid bromine to phosphorus tribromide at 0 °C, followed by the slow addition of water and vacuum distillation of the resulting slurry.

  7. Tribromide - Wikipedia

    en.wikipedia.org/wiki/Tribromide

    Tribromide is the anion with the chemical formula Br 3 −, or salts containing it: . Tetrabutylammonium tribromide; Tetrabromophosphonium tribromide; Pyridinium perbromide; Sodium and potassium tribromides can be prepared by reacting NaBr or KBr with aqueous bromine.

  8. Hell–Volhard–Zelinsky halogenation - Wikipedia

    en.wikipedia.org/wiki/Hell–Volhard–Zelinsky...

    An example of the Hell–Volhard–Zelinsky reaction can be seen in the preparation of alanine from propionic acid.In the first step, a combination of bromine and phosphorus tribromide is used in the Hell–Volhard–Zelinsky reaction to prepare 2-bromopropionic acid, [3] which in the second step is converted to a racemic mixture of the amino acid product by ammonolysis.

  9. Phosphorus trichloride - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_trichloride

    Phosphorus tribromide Phosphorus triiodide: Supplementary data page ... PCl 3 as an electrophile. PCl 3 reacts vigorously with water to form phosphorous acid ...