Dichlorophenylphosphine

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Dichlorophenylphosphine
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Dichlorophenylphosphine-3D-balls-by-AHRLS-2012.png
Names
Preferred IUPAC name
Phenylphosphonous dichloride
Other names
Dichlorophenylphosphane
Phenylphosphorus dichloride
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.010.388 Edit this at Wikidata
EC Number
  • 211-425-8
RTECS number
  • TB2478000
UNII
UN number 2798
Properties
C6H5Cl2P
Molar mass 178.98 g·mol−1
Appearance colorless liquid
Odor acrid, pungent
Density 1.3190 g/mL
Melting point −51 °C (−60 °F; 222 K)
Boiling point 222 °C (432 °F; 495 K)
insoluble
Solubility miscible in benzene, CS2, chloroform
1.6030
Hazards
Safety data sheet Fisher MSDS
GHS pictograms GHS05: CorrosiveGHS06: ToxicGHS07: Harmful
GHS Signal word Danger
GHS hazard statements
H290, H301, H302, H314, H318, H335
P234, P260, P261, P264, P270, P271, P280, P301+310, P301+312, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P312, P321, P330, P363, P390, P403+233, P404, P405, P501
NFPA 704 (fire diamond)
3
1
3
W
Flash point 101 °C (214 °F; 374 K)
159 °C (318 °F; 432 K)
Lethal dose or concentration (LD, LC):
LD50 (median dose)
200 mg/kg (oral, rat)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Dichlorophenylphosphine is an organophosphorus compound with the formula C6H5PCl2. This colourless viscous liquid is commonly used in the synthesis of phosphine ligands.

Dichlorophenylphosphine is commercially available. It may be prepared by an electrophilic substitution of benzene by phosphorus trichloride, catalyzed by aluminium chloride.[1] The compound is an intermediate for the synthesis of other chemicals for instance dimethylphenylphosphine: DOI:

C6H5PCl2 + 2 CH3MgI → C6H5P(CH3)2 + 2 MgICl

In the McCormack reaction dichlorophenylphosphine adds dienes to give the chlorophospholenium ring.[2]

McCormackRxn.png


References[]

  1. ^ B. Buchner, L. B. Lockhart, Jr. (1951). "Phenyldichlorophosphine". 31: 88. doi:10.15227/orgsyn.031.0088. Cite journal requires |journal= (help)CS1 maint: multiple names: authors list (link)
  2. ^ W. B. McCormack (1963). "3-Methyl-1-Phenylphospholene oxide". Org. Synth. 43: 73. doi:10.15227/orgsyn.043.0073.
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