Dichlorophenylphosphine

This colourless viscous liquid is commonly used in the synthesis of organophosphines.

It may be prepared by an electrophilic substitution of benzene by phosphorus trichloride, catalyzed by aluminium chloride.

[2] The compound is an intermediate for the synthesis of other chemicals for instance dimethylphenylphosphine: Many tertiary phosphines can be prepared by this route.

[3] In the McCormack reaction dichlorophenylphosphine adds dienes to give the chlorophospholenium ring.

[4] Reductive coupling of the dichlorophosphine gives the cyclophosphine (PhP)5.

NFPA 704 four-colored diamond Health 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gas Flammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oil Instability 3: Capable of detonation or explosive decomposition but requires a strong initiating source, must be heated under confinement before initiation, reacts explosively with water, or will detonate if severely shocked. E.g. hydrogen peroxide Special hazard W: Reacts with water in an unusual or dangerous manner. E.g. sodium, sulfuric acid