Бензоилхлорид — Википедия
Бензоилхлорид — ВикипедияБензоилхлорид — Википедия
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Benzoyl chloride , also known as benzenecarbonyl chloride , is an organochlorine compound with the formula C 6 H 5 COCl. It is a colourless, fuming liquid with an irritating odour. It is mainly useful for the production of peroxides but is generally useful in other areas such as in the preparation of dyes , perfumes , pharmaceuticals , and resins. Benzoyl chloride is produced from benzotrichloride using either water or benzoic acid: As with other acyl chlorides , it can be generated from the parent acid and other chlorinating agents phosphorus pentachloride or thionyl chloride. It was first prepared by treatment of benzaldehyde with chlorine. An early method for production of benzoyl chloride involved chlorination of benzyl alcohol. It reacts with water to produce hydrochloric acid and benzoic acid:. Benzoyl chloride is a typical acyl chloride. It reacts with alcohols to give the corresponding esters. Similarly, it reacts with amines to give the amide. It undergoes the Friedel-Crafts acylation with aromatic compounds to give the corresponding benzophenones and related derivatives. Benzoyl peroxide , a common reagent in polymer chemistry , is produced industrially by treating benzoyl chloride with hydrogen peroxide and sodium hydroxide: From Wikipedia, the free encyclopedia. Not to be confused with benzyl chloride. Interactive image Interactive image. Lazier 'Benzoyl Piperidine' Org. Hiyama 'Directed Reduction of a beta-keto Amide: Erythro 3-hydroxymethylphenylpropanoyl piperidine' Org. Retrieved 31 October Retrieved from ' https: Views Read Edit View history. In other projects Wikimedia Commons. This page was last edited on 4 July , at By using this site, you agree to the Terms of Use and Privacy Policy.
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Бензоилхлорид
Большая советская энциклопедия - бензоилхлорид
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