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  2. Phthalic anhydride - Wikipedia

    en.wikipedia.org/wiki/Phthalic_anhydride

    Phthalic anhydride is the organic compound with the formula C 6 H 4 (CO) 2 O. It is the anhydride of phthalic acid. Phthalic anhydride is a principal commercial form of phthalic acid. It was the first anhydride of a dicarboxylic acid to be used commercially. This white solid is an important industrial chemical, especially for the large-scale ...

  3. Phthalimide - Wikipedia

    en.wikipedia.org/wiki/Phthalimide

    Phthalimide is the organic compound with the formula C 6 H 4 (CO) 2 NH. It is the imide derivative of phthalic anhydride. It is a sublimable white solid that is slightly soluble in water but more so upon addition of base. It is used as a precursor to other organic compounds as a masked source of ammonia. [2]

  4. Deprotonation - Wikipedia

    en.wikipedia.org/wiki/Deprotonation

    The hydrogen is dangerous and could ignite with the oxygen in the air, so the chemical procedure should be done in an inert atmosphere (e.g., nitrogen). Deprotonation can be an important step in a chemical reaction. Acid–base reactions typically occur faster than any other step which may determine the product of a reaction. The conjugate base ...

  5. N-Hydroxyphthalimide - Wikipedia

    en.wikipedia.org/wiki/N-Hydroxyphthalimide

    N-Hydroxyphthalimide is the organic compound with the formula C6H4(CO)2NOH. A white or yellow solid, it is a derivative of phthalimide. The compound is as a catalyst in the synthesis of other organic compounds. [1][2] It is soluble in water and organic solvents such as acetic acid, ethyl acetate and acetonitrile. [3]

  6. Vanadium(V) oxide - Wikipedia

    en.wikipedia.org/wiki/Vanadium(V)_oxide

    Vanadium (V) oxide (vanadia) is the inorganic compound with the formula V 2 O 5. Commonly known as vanadium pentoxide, it is a brown/yellow solid, although when freshly precipitated from aqueous solution, its colour is deep orange. Because of its high oxidation state, it is both an amphoteric oxide and an oxidizing agent.

  7. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    Friedel–Crafts reactions have been used in the synthesis of several triarylmethane and xanthene dyes. [26] Examples are the synthesis of thymolphthalein (a pH indicator) from two equivalents of thymol and phthalic anhydride: A reaction of phthalic anhydride with resorcinol in the presence of zinc chloride gives the fluorophore fluorescein.

  8. Phthalic acid - Wikipedia

    en.wikipedia.org/wiki/Phthalic_acid

    In organic chemistry, phthalic acid is an aromatic dicarboxylic acid, with formula C6H4(CO2H)2 and structure HO (O)C− C 6 H 4− C (O)OH. Although phthalic acid is of modest commercial importance, the closely related derivative phthalic anhydride is a commodity chemical produced on a large scale. [4] Phthalic acid is one of three isomers of ...

  9. Beckmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Beckmann_rearrangement

    The Beckmann rearrangement, named after the German chemist Ernst Otto Beckmann (1853–1923), is a rearrangement of an oxime functional group to substituted amides. [ 1 ][ 2 ] The rearrangement has also been successfully performed on haloimines and nitrones. Cyclic oximes and haloimines yield lactams.