Benzoyl chloride, also known as benzenecarbonyl chloride, is an organochlorine compound with the formula C7H5ClO. It is a colourless, fuming liquid with an irritating odour, and consists of a benzene ring (C6H6) with an acyl chloride (−C(=O)Cl) substituent. 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.
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| Names | |||
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| Preferred IUPAC name
Benzoyl chloride | |||
| Other names
Benzoic acid chloride (1:1)
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| Identifiers | |||
3D model (JSmol)
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| ECHA InfoCard | 100.002.464 | ||
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| UNII | |||
| UN number | 1736 | ||
CompTox Dashboard (EPA)
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| Properties | |||
| C7H5ClO | |||
| Molar mass | 140.57 g·mol−1 | ||
| Appearance | colorless liquid | ||
| Odor | Benzaldehyde like but more pungent | ||
| Density | 1.21 g/mL, liquid | ||
| Melting point | −1 °C (30 °F; 272 K) | ||
| Boiling point | 197.2 °C (387.0 °F; 470.3 K) | ||
| reacts, forms hydrogen chloride on contact with water | |||
| -75.8·10−6 cm3/mol | |||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
Main hazards
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Maybe harmful by ingestion and skin absorption; possible carcinogen[1] | ||
| GHS labelling: | |||
 
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| Danger | |||
| H302, H312, H314, H317, H332 | |||
| P260, P261, P264, P270, P271, P272, P280, P301 P312, P301 P330 P331, P302 P352, P303 P361 P353, P304 P312, P304 P340, P305 P351 P338, P310, P312, P321, P322, P330, P333 P313, P363, P405, P501 | |||
| NFPA 704 (fire diamond) | |||
| Flash point | 72 °C (162 °F; 345 K) | ||
| Safety data sheet (SDS) | Fisher Scientific MSDS | ||
| Related compounds | |||
Related compounds
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benzoic acid, benzoic anhydride, benzaldehyde | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Preparation
editBenzoyl chloride is produced from benzotrichloride using either water or benzoic acid:[2]
- C6H5CCl3 H2O → C6H5COCl 2 HCl
- C6H5CCl3 C6H5CO2H → 2 C6H5COCl HCl
As with other acyl chlorides, it can be generated from the parent acid and standard chlorinating agents such as phosphorus pentachloride, thionyl chloride, and oxalyl chloride. It was first prepared by treatment of benzaldehyde with chlorine.[3]
An early method for production of benzoyl chloride involved chlorination of benzyl alcohol.[4]
Reactions
editIt reacts with water to produce hydrochloric acid and benzoic acid:
- C6H5COCl H2O → C6H5COOH HCl
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.[5][6]
It undergoes the Friedel-Crafts acylation with aromatic compounds to give the corresponding benzophenones and related derivatives.[7] With carbanions, it serves again as a source of the benzoyl cation synthon, C6H5CO .[8]
Benzoyl peroxide, a common reagent in polymer chemistry, is produced industrially by treating benzoyl chloride with hydrogen peroxide and sodium hydroxide:[9]
- 2 C6H5COCl H2O2 2 NaOH → (C6H5CO)2O2 2 NaCl 2 H2O
References
edit- ^ Benzoyl chloride: toxicity and precautions
- ^ Maki, Takao; Takeda, Kazuo (2000). "Benzoic Acid and Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_555. ISBN 3527306730.
- ^ Friedrich Wöhler, Justus von Liebig (1832). "Untersuchungen über das Radikal der Benzoesäure". Annalen der Pharmacie. 3 (3): 262–266. doi:10.1002/jlac.18320030302. hdl:2027/hvd.hxdg3f.
- ^ US1851832, 29 March 1932
- ^ Marvel, C. S.; Lazier, W. A. (1929). "Benzoyl Piperidine". Organic Syntheses. 9: 16. doi:10.15227/orgsyn.009.0016.
- ^ Prasenjit Saha, Md Ashif Ali, and Tharmalingam Punniyamurthy "Ligand-free Copper(ii) Oxide Nanoparticles Catalyzed Synthesis Of Substituted Benzoxazoles" Org. Synth. 2011, volume 88, pp. 398. doi:10.15227/orgsyn.088.0398. (an illustrative reaction of an amine with benzoyl chloride).
- ^ Minnis, Wesley (1932). "Phenyl Thienyl Ketone". Organic Syntheses. 12: 62. doi:10.15227/orgsyn.012.0062.
- ^ Fujita, M.; Hiyama, T. (1990). "Directed Reduction of a beta-keto Amide: Erythro-1-(3-hydroxy-2-methyl-3-phenylpropanoyl)piperidine". Organic Syntheses. 69: 44. doi:10.15227/orgsyn.069.0044.
- ^ El-Samragy, Yehia (2004). "Chemical and Technical Assessment". Benzoyl Peroxide (PDF). 61st JECFA (Technical report). Joint FAO/WHO Expert Committee on Food Additives. p. 1. Retrieved 31 October 2013.