Benzyl bromide is an organic compound with the formula C6H5CH2Br. The molecule consists of a benzene ring substituted with a bromomethyl group. It is a colorless liquid with lachrymatory properties. The compound is a reagent for introducing benzyl groups.[3][4]
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| Names | |||
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| Preferred IUPAC name
(Bromomethyl)benzene | |||
| Other names
α-Bromotoluene | |||
| Identifiers | |||
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| ECHA InfoCard | 100.002.589 
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PubChem CID |
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| Properties | |||
| C7H7Br | |||
| Molar mass | 171.037 g·mol−1 | ||
| Appearance | Colorless liquid | ||
| Odor | Sharp and pungent | ||
| Density | 1.438 g/cm3 | ||
| Melting point | −3.9 °C (25.0 °F; 269.2 K) | ||
| Boiling point | 201 °C (394 °F; 474 K) | ||
| Solubility | organic solvents | ||
| log P | 2.92[2] | ||
Refractive index (nD) |
1.5752 | ||
| Hazards | |||
| GHS labelling: | |||
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| Flash point | 70 °C (158 °F; 343 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
Benzyl bromide can be synthesized by the bromination of toluene under conditions suitable for a free radical halogenation:
The structure has been examined by electron diffraction.[5]
Benzyl bromide is used in organic synthesis for the introduction of the benzyl groups when the less expensive benzyl chloride is insufficiently reactive.[6] [7] Benzylations are often achieved in the presence of catalytic amounts of sodium iodide, which generates the more reactive benzyl iodide in situ.[3] In some cases, benzyl serves as protecting group for alcohols and carboxylic acids.[8]
Benzyl bromide is a strong lachrymator and is also intensely irritating to skin and mucous membranes. Because of these properties, it has been used in chemical warfare, both in combat and in training due to its irritating yet non-lethal nature.
