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  2. Benzoyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_chloride

    Benzoyl chloride is produced from benzotrichloride using either water or benzoic acid: [2] C 6 H 5 CCl 3 + H 2 O → C 6 H 5 COCl + 2 HCl C 6 H 5 CCl 3 + C 6 H 5 CO 2 H → 2 C 6 H 5 COCl + HCl. As with other acyl chlorides, it can be generated from the parent acid and standard chlorinating agents such as phosphorus pentachloride, thionyl ...

  3. 4-Chlorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Chlorobenzaldehyde

    It can be produced by hydrolysis of 4-chlorobenzal chloride: [2]. ClC 5 H 4 CHCl 2 + H 2 O → ClC 5 H 4 CHO + 2 HCl. It can also be produced by the oxidation of 4-chlorobenzyl alcohol.

  4. 2,4,6-Trichlorobenzoyl chloride - Wikipedia

    en.wikipedia.org/.../2,4,6-Trichlorobenzoyl_chloride

    This produces 2,4,6-trichlorobenzoic acid, which can then be refluxed in thionyl chloride to form 2,4,6-trichlorobenzoyl chloride. [ 4 ] Since 2,4,6-trichlorobenzoic acid is produced as a by product of the Yamaguchi esterification process, it can be refluxed again to recreate 2,4,6-trichlorobenzoyl chloride.

  5. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    Benzoic acid (/ b ɛ n ˈ z oʊ. ɪ k /) is a white (or colorless) solid organic compound with the formula C 6 H 5 COOH, whose structure consists of a benzene ring (C 6 H 6) with a carboxyl (−C(=O)OH) substituent.

  6. Benzyl bromide - Wikipedia

    en.wikipedia.org/wiki/Benzyl_bromide

    Benzyl bromide is an organic compound with the formula C 6 H 5 CH 2 Br. The molecule consists of a benzene ring substituted with a bromomethyl group. It is a colorless liquid with lachrymatory properties.

  7. Benzyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloroformate

    Benzyl chloroformate, also known as benzyl chlorocarbonate or Z-chloride, is the benzyl ester of chloroformic acid. It can be also described as the chloride of the benzyloxycarbonyl (Cbz or Z) group. In its pure form it is a water-sensitive oily colorless liquid, although impure samples usually appear yellow.

  8. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Benzyl ethers are often derived from benzyl chloride. Benzyl chloride reacts with aqueous sodium hydroxide to give dibenzyl ether. In organic synthesis, benzyl chloride is used to introduce the benzyl protecting group in reaction with alcohols, yielding the corresponding benzyl ether, carboxylic acids, and benzyl ester. Benzoic acid (C 6 H 5 ...

  9. 4-Chlorophenol - Wikipedia

    en.wikipedia.org/wiki/4-Chlorophenol

    4-Chlorophenol is an organic compound with the formula C 6 H 4 ClOH. It is one of three monochlorophenol isomers. It is a colorless or white solid that melts easily and exhibits significant solubility in water.