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Allyl chloride is the organic compound with the formula CH<sub>2</sub>=CHCH<sub>2</sub>Cl. This colorless liquid is insoluble in water but soluble in common organic solvents. It is mainly converted to epichlorohydrin, used in the production of plastics. It is a chlorinated derivative of propylene. It is an alkylating agent, which makes it both useful and hazardous to handle. Modern preparation protocols economize this approach, replacing relatively expensive phosphorus trichloride with hydrochloric acid and a catalyst such as copper(I) chloride.

Industrial scale

Allyl chloride is produced by the chlorination of propylene. At lower temperatures, the main product is 1,2-dichloropropane, but at 500&nbsp;°C, allyl chloride predominates, being formed via a free radical reaction:

:<chem>CH3CH=CH2 + Cl2 -> ClCH2CH=CH2 + HCl</chem>

An estimated 800,000 tonnes were produced this way in 1997. and 1-bromo-3-chloropropane.

As an alkylating agent, it is useful in the manufacture of pharmaceuticals and pesticides, such as mustard oil.

Illustrative reactions

Illustrative of its reactivity is its cyanation to allyl cyanide (CH<sub>2</sub>=CHCH<sub>2</sub>CN). Being a reactive alkyl halide, it undergoes reductive coupling to give diallyl:

:<chem>2 ClCH2CH=CH2 + Mg -> (CH2)2(CH=CH2)2 + MgCl2</chem>

It undergoes oxidative addition to palladium(0) to give allylpalladium chloride dimer, (C<sub>3</sub>H<sub>5</sub>)<sub>2</sub>Pd<sub>2</sub>Cl<sub>2</sub>. Dehydrohalogenation gives cyclopropene.

Safety

Allyl chloride is highly toxic and flammable. Eye effects may be delayed and may lead to possible impairment of vision.

See also

  • Allyl
  • Allyl bromide
  • Allyl iodide
  • IARC Monograph *Allyl chloride.

References