Methylenetriphenylphosphorane

Methylenetriphenylphosphorane
Names


IUPAC name Methylene(triphenyl)phosphorane
Identifiers
CAS Number	3487-44-3
3D model (Jmol)	Interactive image
ChemSpider	121606
PubChem CID	137960
InChI InChI=1S/C19H17P/c1-20(17-11-5-2-6-12-17,18-13-7-3-8-14-18)19-15-9-4-10-16-19/h2-16H,1H2 Key: XYDYWTJEGDZLTH-UHFFFAOYSA-N InChI=1/C19H17P/c1-20(17-11-5-2-6-12-17,18-13-7-3-8-14-18)19-15-9-4-10-16-19/h2-16H,1H2 Key: XYDYWTJEGDZLTH-UHFFFAOYAU
SMILES C=P(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3
Properties
Chemical formula	C₁₉H₁₇P
Appearance	yellow solid
Density	1.19 g/cm³
Solubility in water	decompose
Solubility	THF
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Methylenetriphenylphosphorane is an organophosphorus compound with the formula Ph₃PCH₂. It is the parent member of the phosphorus ylides, popularly known as Wittig reagents. It is a highly polar, highly basic species.

Methylenetriphenylphosphorane is prepared from triphenylphosphine and methyl bromide followed by deprotonation of the resulting phosphonium salt using a strong base like butyllithium:

The compound is generally not isolated, instead it is used in situ.

Methylenetriphenylphosphorane is used to replace oxygen centres in aldehydes and ketones with a methylene group:

The phosphorus-containing product is triphenylphosphine oxide.

Crystallographic characterization of the colourless ylide reveals that the phosphorus atom is approximately tetrahedral. The PCH₂ centre is planar and the P=CH₂ distance is 1.661 Å, which is much shorter than the P-Ph distances (1.823 Å). The compound is usually described as a combination of two resonance structures:

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