Chemistry:Methyltriphenylphosphonium bromide

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Methyltriphenylphosphonium bromide
Ph3PCH3+Br-.png
Names
Preferred IUPAC name
Methyltri(phenyl)phosphanium bromide
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
EC Number
  • 217-218-9
UNII
Properties
C19H18BrP
Molar mass 357.231 g·mol−1
Appearance white solid
Hazards
GHS pictograms GHS06: ToxicGHS07: HarmfulGHS09: Environmental hazard
GHS Signal word Danger
H300, H301, H302, H312, H315, H319, H332, H411
P261, P264, P270, P271, P273, P280, P301+310, P301+312, P302+352, P304+312, P304+340, P305+351+338, P312, P321, P322, P330, P332+313, P337+313, P362, P363, P391, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Methyltriphenylphosphonium bromide is the organophosphorus compound with the formula [(C6H5)3PCH3]Br. It is the bromide salt of a phosphonium cation. It is a white salt that is soluble in polar organic solvents.

Synthesis and reactions

Methyltriphenylphosphonium bromide is produced by treating triphenylphosphine with methyl bromide:[1]

Ph3P + CH3Br → Ph3PCH3Br

Methyltriphenylphosphonium bromide is the principal precursor to methylenetriphenylphosphorane, a useful methylenating reagent. This conversion is achieved by treating methyltriphenylphosphonium bromide with strong base.[2]

Ph3PCH3Br + BuLi → Ph3PCH2 + LiBr + BuH

References

  1. Wittig, Georg; Schoellkopf, U. (1960). "Methylenecyclohexane". Organic Syntheses 40: 66. doi:10.15227/orgsyn.040.0066. 
  2. Fitjer, Lutz; Quabeck, Ulrike (1985). "The Wittig Reaction Using Potassium-tert-butoxide High Yield Methylenations of Sterically Hindered Ketones". Synthetic Communications 15 (10): 855–864. doi:10.1080/00397918508063883.