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Allyl chloride

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Formula
  
C3H5Cl

Boiling point
  
45.1 °C

Density
  
940 kg/m³


Appearance
  
Colorless, brown, yellow, or purple liquid

Allyl chloride meaning


Allyl chloride is the organic compound with the formula CH2=CHCH2Cl. 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.

Contents

Allyl chloride Allyl chloride Wikipedia

Isothermal yield of allyl chloride versus conversion of propylene


Laboratory scale

Allyl chloride SN2 Reaction Allyl Chloride with HS is loaded

Allyl chloride was first produced in 1857 by Auguste Cahours and August Hofmann by reacting allyl alcohol with phosphorus trichloride. 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 Allyl Chloride

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

CH3CH=CH2 + Cl2 → ClCH2CH=CH2 + HCl

An estimated 800,000 metric tons were produced this way in 1997.

Reactions and uses

Allyl chloride Coproduction of allyl chloride amp 13dichloropropene soil fumigant

The great majority of allyl chloride is converted to epichlorohydrin. Other commercially significant derivatives include allyl alcohol, allylamine, allyl isothiocyanate (synthetic mustard oil) and allylsilane.

Allyl chloride httpsuploadwikimediaorgwikipediacommonsthu

As an alkylating agent, it is useful in the manufacture of pharmaceuticals and pesticides, such as mustard oil. Illustrative of its reactivity is its cyanation to allyl cyanide (CH2=CHCH2CN), reductive coupling to give diallyl, oxidative addition to palladium to give allylpalladium chloride dimer, (C3H5)2Pd2Cl2, and dehydrohalogenation to cyclopropene.

Safety

Allyl chloride 107051 CAS ALLYL CHLORIDE Allyl Halides Article No 00877

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

Allyl chloride Allyl chloride reagent grade 98 SigmaAldrich

Allyl chloride allyl chloride C3H5Cl ChemSpider


Allyl chloride Patent US3865886 Production of allyl chloride Google Patents

References

Allyl chloride Wikipedia