Trimethyl phosphite
Names
Preferred IUPAC name
Trimethyl phosphite[1]
Other names
Trimethoxyphosphine
Trimethoxyphosphane
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.004.065 Edit this at Wikidata
UNII
  • InChI=1S/C3H9O3P/c1-4-7(5-2)6-3/h1-3H3 checkY
    Key: CYTQBVOFDCPGCX-UHFFFAOYSA-N checkY
  • InChI=1/C3H9O3P/c1-4-7(5-2)6-3/h1-3H3
    Key: CYTQBVOFDCPGCX-UHFFFAOYAO
  • COP(OC)OC
Properties
C3H9O3P
Molar mass 124.08
Appearance colorless liquid
Odor distinctive, pungent[2]
Density 1.052
Melting point −78 °C (−108 °F; 195 K)
Boiling point 111 °C (232 °F; 384 K)
reacts[2]
Vapor pressure 24 mmHg (25°C)[2]
Hazards
Flash point 28 °C; 82 °F; 301 K[2]
NIOSH (US health exposure limits):
PEL (Permissible)
 none[2]
REL (Recommended)
 TWA 2 ppm (10 mg/m3)[2]
IDLH (Immediate danger)
 N.D.[2]
Related compounds
Related compounds
 Dimethyl methylphosphonate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Trimethyl phosphite is an organophosphorus compound with the formula P(OCH3)3, often abbreviated P(OMe)3. It is a colorless liquid with a highly pungent odor. It is the simplest phosphite ester and finds used as a ligand in organometallic chemistry and as a reagent in organic synthesis. The molecule features a pyramidal phosphorus(III) center bound to three methoxy groups.

Synthesis

Trimethyl phosphite is in principle obtainable by methanolysis of phosphorus trichloride, say in the presence of a proton accepting base. This method suffers from numerous side reactions however. The use of sodium methoxide is superior:[3]

PCl3 + 3 NaOCH3 → P(OCH3)3 + 3 NaCl

Reactions

Trimethyl phosphite is susceptible to oxidation to trimethyl phosphate:

P(OCH3)3 + 0.5 O2 → OP(OCH3)3

It reacts with a catalytic amount of methyl iodide in the Arbuzov reaction to give dimethyl methylphosphonate:

P(OCH3)3 → CH3P(O)(OCH3)2

As a ligand, trimethyl phosphite has a smaller cone angle and better acceptor properties relative to trimethylphosphine. A representative derivative is the colorless tetrahedral complex Ni(P(OMe)3)4 (m.p. 108 °C).[4] The tridentate ligand called the Kläui ligand is derived from trimethyl phosphite. The formation of this ligand illustrates the susceptibility of trimethyl phosphite (and metal complexes thereof) to the Arbuzov reaction.

Trimethyl phosphite is also used as a mild desulfurization reagent in organic synthesis, for example in the preparation of derivatives of tetrathiafulvalene.[5]

Toxicity

The LD50 is 1600–2890 mg/kg (oral, rat).[6]

References

  1. ^ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 931. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
  2. ^ a b c d e f g NIOSH Pocket Guide to Chemical Hazards. "#0640". National Institute for Occupational Safety and Health (NIOSH).
  3. ^ Crofts, Peter C.; Kosolapoff, Gennady M. (1953). "Preparation and Determination of Apparent Dissociation Constants of Some Alkylphosphonic and Dialkylphosphinic Acids1". Journal of the American Chemical Society. 75 (14): 3379–3383. doi:10.1021/ja01110a024.
  4. ^ Steven D. Ittel; Cushing, M. A. (1990). Complexes of Nickel(0). Inorganic Syntheses. Vol. 28. pp. 98–104. doi:10.1002/9780470132593.ch25. ISBN 978-0-471-52619-3.
  5. ^ Larsen, Jan; Lenoir, Christine (1995). "2,2'-Bi-5,6-Dihydro-1,3-Dithiolo[4,5-b][1,4]dithiinylidene (BEDT-TTF)". Org. Synth. 72: 265. doi:10.15227/orgsyn.072.0265.
  6. ^ 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.

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