Benzyl chloride

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Benzyl chloride
Benzyl chloride     100px
Chemical name Chloromethylbenzene
Chemical formula C7H7Cl
Molecular mass 126.59 g/mol
CAS number [100-44-7]
Density 1.100 g/cm3
Melting point -39 °C
Boiling point 179 °C
SMILES ClCC1=CC=CC=C1
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Benzyl chloride, or α-chlorotoluene, is an organic compound consisting of a phenyl group substituted with a chloromethyl group. It can be prepared by the chlorination of toluene.

Benzyl chloride is used in organic synthesis for the introduction of the benzyl protecting group for alcohols (yielding the corresponding benzyl ether) and carboxylic acids (yielding the corresponding benzyl ester). It may be used in the synthesis of amphetamine-class drugs, and for this reason sales of benzyl chloride are monitored as a List II drug precursor chemical by the Drug Enforcement Administration in the United States of America.

Benzyl chloride reacts with water in a hydrolysis reaction to form benzyl alcohol and hydrogen chloride. When the latter is dissolved in water, it forms hydrochloric acid. Since benzyl chloride is quite volatile at room temperature, it can easily reach the mucous membranes where the hydrolysis takes place with production of hydrochloric acid. This explains why benzyl chloride is a lachrymator and has been used as a war gas. It is also very irritating to the skin.

Benzyl chloride also reacts readily with metallic magnesium to produce a Grignard Reagent.

A commonly used parent compound is benzyl bromide.

See also

External links

Template:Organohalide-stub fi:Bentsyylikloridi de:Benzylchlorid



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