Diphenylphosphine
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| Preferred IUPAC name Diphenylphosphane | |
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| ECHA InfoCard | 100.011.447  |
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Chemical formula | C12H11P |
| Molar mass | 186.19 g/mol |
| Appearance | colorless liquid |
| Density | 1.07 g/cm3, liquid |
| Boiling point | 280 °C (536 °F; 553 K) |
Solubility in water | Insoluble |
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Hazard statements | H250, H315, H319, H335 |
Precautionary statements | P210, P222, P261, P264, P271, P280, P302+P334, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P405, P422, P501 |
| Safety data sheet (SDS) | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).  Y verify (what is  Y N ?) Infobox references | |
Chemical compound
Diphenylphosphine, also known as diphenylphosphane, is an organophosphorus compound with the formula (C6H5)2PH. This foul-smelling, colorless liquid is easily oxidized in air. It is a precursor to organophosphorus ligands for use as catalysts.
Synthesis
Diphenylphosphine can be prepared from triphenylphosphine by reduction to lithium diphenylphosphide, which can be protonated to give the title compound:[1]
- PPh3 + 2 Li → LiPPh2 + LiPh
- LiPPh2 + H2O → Ph2PH + LiOH
Uses and reactions
In the laboratory, diphenylphosphine is a common intermediate. It can be deprotonated to give diphenylphosphide derivatives:[2]
- Ph2PH + nBuLi → Ph2PLi + nBuH
The preparation of phosphine ligands, Wittig-Horner reagents, and phosphonium salts are commonly accomplished by alkylating diphenylphosphine. The hydrogen atom connected to phosphorus undergoes Michael-like addition to activated alkenes, providing products with which to produce phosphine ligands such as 1,2-bis(diphenylphosphino)ethane (Ph2PC2H4PPh2) and BINAP.[3] via its bistriflate derivatives. Both the (R)- and (S)-enantiomers, as well as the racemate, are commercially available. One of the wide applications include chemoselective hydrogenation, where BINAP is conjugated to rhodium.
Diphenylphosphine and especially diphenylphosphide derivatives are nucleophiles, so they add to carbon – heteroatom double bonds.[2] For example, in the presence of concentrated hydrochloric acid at 100 °C, diphenylphosphine adds to the carbon atom in benzaldehyde to give (phenyl-(phenylmethyl)phosphoryl)benzene.
- Ph2PH + PhCHO → Ph2P(O)CH2Ph
Compared to tertiary phosphines, diphenylphosphine is weakly basic. The pKa of the protonated derivative is 0.03:[4]
- Ph2PH2+ ⇌ Ph2PH + H+
Handling properties
Diphenylphosphine readily oxidizes.[5]
- Ph2PH + O2 → Ph2P(O)OH
An intermediate in this oxidation is diphenylphosphine oxide. The use of the diphenylphosphine–borane complex, Ph2PH•BH3 avoids the problem of phosphine oxidation by protecting the phosphine from oxidation and is available through chemical vendors.[2]
References
- ^ V. D. Bianco; S. Doronzo (1976). Diphenylphosphine. Inorganic Syntheses. Vol. 16. pp. 161–188. doi:10.1002/9780470132470.ch43. ISBN 9780470132470.
- ^ a b c Piotrowski, D. W. (2001). "Diphenylphosphine". Encyclopedia of Reagents for Organic Synthesis. New York: John Wiley & Sons. doi:10.1002/047084289X.rd427. ISBN 0471936235.
- ^ Cai, Dongwei; J. F. Payack; D. R. Bender; D. L. Hughes; T. R. Verhoeven; P. J. Reider (1999). "(R)-(+)- and (S)-(−)-2,2′-bis(diphenylphosphino)-1,1′-binapthyl (BINAP)". Organic Syntheses. 76: 6.
- ^ C. A. Streuli, "Determination of Basicity of Substituted Phosphines by Nonaqueous Titrimetry", Analytical Chemistry 1960, volume 32, pages 985-987.doi:10.1021/ac60164a027
- ^ Svara, J.; Weferling, N.; Hofmann, T. "Phosphorus Compounds, Organic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_545.pub2. ISBN 978-3527306732.
