Chemistry:P4-t-Bu

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P4-t-Bu
P4-t-Bu Strukturformel.svg
Identifiers
3D model (JSmol)
UNII
Properties
(CH
3)
3C–N=P(–N=P(–N(CH
3)
2)
3)
3
Molar mass 633.732 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Tracking categories (test):

P4-t-Bu is a readily accessible chemical from the group of neutral, peralkylated sterically hindered polyaminophosphazenes, which are extremely strong bases but very weak nucleophiles, with the formula (CH
3)
3C–N=P(–N=P(–N(CH
3)
2)
3)
3. "t-Bu" stands for tert-butyl (CH
3)
3C–. "P4" stands for the fact that this molecule has 4 phosphorus atoms. P4-t-Bu can also be regarded as tetrameric triaminoiminophosphorane of the basic structure H–N=P(–NH
2)
3. The homologous series of P1 to P7 polyaminophosphazenes[1][2] of the general formula [math]\ce{ [(R^1_2N)_3P=N-]_\mathit{x}-(R^1_2N)_{3\!-\mathit{x}}P=NR2 }[/math] with preferably methyl groups as R1, a methyl group or tert-butyl group as and even-numbered x between 0 and 6 (P4-t-Bu: R1 = Me, R2 = t-Bu and x = 3)[3] has been developed by Reinhard Schwesinger; the resulting phosphazene bases are therefore also referred to as Schwesinger superbases.[4][5]

Preparation

The convergent synthesis of P4-t-Bu[6] is derived from phosphorus pentachloride (1) and leads in branch [A] to the well-characterized aminotris via the non-isolated chlorine (dimethylamino)phosphonium chloride (2)[2] via [(Dimethylamino)phosphonium tetrafluoroborate (3) and further via [A2] to the liquid iminotris (dimethylamino) phosphorane[7](4)

[math]\displaystyle{ \begin{matrix}{}\\ \underbrace\ce{PCl5}_{(1)}\ \ce{-\gt [\ce{Me2NH}]} \underbrace{\left[ \ce{(Me2N)3\overset{\oplus}P-Cl . \overset{\ominus}Cl} \right]}_{(2)}\ \ce{-\gt [1.\ \ce{NH3}][2.\ \ce{NaBF4}]}\ \underbrace\ce{(Me2N)3\overset{\oplus}P-NH2 . \overset{\ominus}BF4}_{(3)} \\{}\end{matrix} }[/math]

 

 

 

 

[A1]

[math]\displaystyle{ \underbrace\ce{(Me2N)3\overset{\oplus}P-NH2 . \overset{\ominus}BF4}_{(3)}\ \ce{-\gt [\ce{KOMe}]}\ \underbrace\ce{(Me2N)3P=NH}_{(4)} }[/math]

 

 

 

 

[A2]

 

 

 

 

[A]

and in branch [B] with phosphorus pentachloride and tert-butylammonium chloride to tert-butylphosphorimide trichloride (5)[8]

[math]\displaystyle{ \underbrace\ce{PCl5}_{(1)}\ \ce{-\gt [t\text{-}\ce{Bu-\overset{\oplus}{NH3}.\overset{\ominus}{Cl}}]}\ \underbrace{t\text{-}\ce{Bu-N=PCl3}}_{(5)} }[/math]

 

 

 

 

[B]

The reaction [C] of excess (4) with (5) yields the hydrochloride of the target product P4-t-Bu (6) in 93% yield

[math]\displaystyle{ \scriptstyle\begin{matrix}{}\\ \underbrace\ce{7(Me2N)3P=NH}_{(4)}\ +\ \underbrace{t\text{-}\ce{Bu-N=PCl3}}_{(5)}\ \ce{-\gt }\ \underbrace{\ce{[(Me2N)3P=N]3P=N\overset{\oplus}H-}t\text{-}\ce{Bu . \overset{\ominus}{Cl}}}_{(6)}\ \ce{-\gt [\ce{NaBF4}]}\ \underbrace{\ce{[(Me2N)3P=N]3P=N\overset{\oplus}H-}t\text{-}\ce{Bu . \overset{\ominus}BF4}}_{(7)}\ \ce{-\gt [\ce{KOMe / NaNH2}]}\ \underbrace{\ce{[(Me2N)3P=N]3P=N\overset{\oplus}H-}t\text{-}\ce{Bu}}_{(8)} \\{}\end{matrix} }[/math]

 

 

 

 

[C]

which is also converted into the tetrafluoroborate salt (7) from which the free base (8) can be obtained almost quantitatively with potassium methoxide/sodium amide[2] or with potassium amide in liquid ammonia.[9] The transfer of the hygroscopic and readily water-soluble hydrochlorides and the liquid free bases into the tetrafluoroborates, which are difficult to solubilize in water, facilitate the handling of the substances considerably.

Konvergente P4-t-Bu-Synthese

 

 

 

 

[D]

The relatively uncomplicated convergent synthesis with easily accessible reactants and very good yields of the intermediates make P4-t-Bu an interesting phosphazene superbase.[10]

Properties

P4-t-Bu is one of the strongest neutral nitrogenous bases with an extrapolated pKa value of 42.1 in acetonitrile and is compared to the strong base DBU with a pKa value of 24.3 by 18 orders of magnitude more basic.[2] The compound is very soluble in non-polar solvents, such as hexane, toluene or tetrahydrofuran, and is usually commercially available as a 0.8 to 1 molar solution in hexane.[10] Already in weakly acidic media protonation produces the extremely delocalized and soft P4-t-Bu-H cation and causes besides a very strong solubilization effect also an extreme acceleration of addition reactions even at temperatures below -78 °C.

P4-t-Bu owes its extraordinarily high basicity with low nucleophilicity to its very high steric hindrance and the involvement of many donor groups in conjugation with the spatially demanding structure of the cation formed by protonation.

P4-t-Bu is an extremely hygroscopic solid which is thermally stable up to 120 °C and chemically stable to (dry) oxygen and bases.[9] Traces of water and protic impurities can be eliminated by addition of bromoethane. The base is both very hydrophilic and very lipophilic and can be recovered easily and almost completely from reaction mixtures by the formation of the sparingly soluble tetrafluoroborate salt.

Because of its extremely weak Lewis basicity, the cation of P4-t-Bu suppresses typical side reactions of metal organyls (such as aldol condensations) as can be caused by lithium amides such as lithium diisopropylamide (LDA).[11]

Applications

The neutral superbase P4-t-Bu is superior to ionic bases if those are sensitive to oxidation or side reactions (such as acylation) when they cause solubility problems or Lewis acid catalysed side reactions (such as aldol reactions, epoxy ring opening etc).

The dehydrohalogenation of n-alkyl bromides yields the alkene, such as the reaction 1-bromooctane with P4-t-Bu which yields 1-octene almost quantitatively (96%) under mild conditions, compared to the potassium tert-butoxide/18-crown-6 system with only 75% yield.[12]

Alkylations on weakly acidic methylene groups (e.g. in the case of carboxylic esters or nitriles) proceed with high yield and selectivity. For example, by the reaction of 8-phenylmenthylphenylacetate with iodoethane in the presence of P4-t-Bu only the monoethyl derivative in the Z configuration is obtained in 95% yield.[13]

Monoethylierung von 8-Phenylmenthyl-phenylacetat

Succinonitrile reacts with iodoethane in the presence of P4-t-Bu in 98% yield to give the tetraethyl derivative without undergoing a Thorpe-Ziegler reaction to form a cyclic α-ketonitrile.[9]

Tetraalkylierung von 1,2-Dinitrilen

Trifluoromethylation of ketones (such as benzophenone) is also possible at room temperature in good yields up to 84% with the inert fluoroform (HFC-23) in the presence of P4-t-Bu and tris(trimethylsilyl)amine.[14]

Trifluormethylierung von Benzophenon mit Fluoroform

Intramolecular cyclization of ortho-alkynylphenyl ethers leads in the presence of P4-t-Bu under mild conditions without metal catalysts to substituted benzofurans.[15]

Cyclisierungen mit P4-t-Bu zu Benzofuranen

Due to its extreme basicity it was suggested early on that P4-t-Bu should be suited as an initiator for anionic polymerization. With the ethyl acetate/P4-t-Bu initiator system, poly(methyl methacrylate) (PMMA) with narrow polydispersity and molar masses up to 40,000 g·mol−1 could be obtained in THF.[11]

Anionische Polymerisation von MMA zu PMMA

Anionic polymerization of Ethylene oxide with the initiator system n-Butyllithium/P4-t-Bu yields well-defined Polyethylene oxides with low polydispersity.[16]

Cyclic siloxanes (such as hexamethylcyclotrisiloxane or decamethylcyclopentasiloxane) can also be polymerized with catalytic amounts of P4-t-Bu and water or silanols as initiators under good molecular weight control to thermally very stable polysiloxanes having decomposition temperatures of >450 °C.[3][17] Because of its extreme basicity, P4-t-Bu eagerly absorbs water and carbon dioxide, both of which inhibit anionic polymerization. Heating to temperatures >100 °C removes CO2 and water and restores the anionic polymerization. The extreme hygroscopy of the phosphazene base P4-t-Bu as a substance and in solutions requires a great effort for storage and handling and prevents its broader use.

References

  1. ↑ R. Schwesinger (1993), "Wie stark und wie gehindert können ungeladene Phosphazene sein?" (in German), Angew. Chem. 105 (9): 1420–1422, doi:10.1002/ange.19931050940 
  2. ↑ 2.0 2.1 2.2 2.3 R. Schwesinger (1996), "Extremely strong, uncharged auxiliary bases; Monomeric and polymer-supported polyaminophosphazenes (P2-P5)", Liebigs Ann. Chem. 1996 (7): 1055–10081, doi:10.1002/jlac.199619960705 
  3. ↑ 3.0 3.1 P. Hupfield, A. Surgenor, R. Taylor, "Polymerization of siloxanes", US patent 6353075, published 2002-03-05
  4. ↑ J. Saame (2016), "Experimental basicities of superbasic phosphonium ylides and phosphazenes", J. Org. Chem. 81 (17): 7349–7361, doi:10.1021/acs.joc.6b00872, PMID 27392255 
  5. ↑ E.D. Nacsa; T.H. Lambert (2015), "Higher-order cyclopropenimine superbases. Direct neutral Bronsted base catalyzed Michael reactions with α-aryl esters", J. Am. Chem. Soc. 137 (32): 10246–10253, doi:10.1021/jacs.5b05033, PMID 26131761 
  6. ↑ Gupta, Vinayak (2010). New synthetic methods for biologically active aromatic heterocycles (PhD thesis). Iowa State University. doi:10.31274/etd-180810-2033.
  7. ↑ T. Nobori et al., "Process of preparing iminotris(dimethylamino)phosphorane", EP patent 0921128, published 2002-09-25
  8. ↑ R. Schwesinger; J. Willaredt; H. Schlemper; M. Keller; D. Schmitt; H. Fritz (1994), "Novel, Very Strong, Uncharged Auxiliary Bases; Design and Synthesis of Monomeric and Polymer-Bound Triaminoiminophosphorane Bases of Broadly Varied Steric Demand", Chem. Ber. 127 (12): 2435–2454, doi:10.1002/cber.19941271215 
  9. ↑ 9.0 9.1 9.2 R. Schwesinger; Y. Kondo (2010), "Phosphazene Base P4-t-Bu", E-EROS Encyclopedia of Reagents for Organic Synthesis, doi:10.1002/047084289X.rp150.pub2, ISBN 978-0471936237 
  10. ↑ 10.0 10.1 "Strong and Hindered Bases in Organic Syntheses" (PDF; 1,2 MB). Sigma-Aldrich. http://www.sigmaaldrich.com/chemistry/chemical-synthesis/learning-center/chemfiles/chemfile-2001-2003/vol-3-no-1.html. Retrieved 2016-12-20. 
  11. ↑ 11.0 11.1 T. Pietzonka, D. Seebach (1993), "Die P4-Phosphazenbase als Teil eines metallfreien Initiatorsystems für die anionische Polymerisation von Methacrylsäuremethylester" (in German), Angew. Chem. 105 (5): 741–742, doi:10.1002/ange.19931050514, Bibcode: 1993AngCh.105..741P 
  12. ↑ R. Schwesinger; H. Schlemper (1987), "Peralkylierte Polyaminophosphazene – extrem starke neutrale Stickstoffbasen" (in German), Angew. Chem. 99 (11): 1212–1214, doi:10.1002/ange.19870991134, Bibcode: 1987AngCh..99.1212S 
  13. ↑ A. Solladié-Cavallo; A.G. Csaky; I. Gantz; J. Suffert (1994), "Diastereoselective Alkylation of 8-Phenylmenthyl Phenylacetate: Aggregated Lithium Enolate versus "Naked" Enolate", J. Org. Chem. 59 (18): 5343–5346, doi:10.1021/jo00097a041 
  14. ↑ S. Okusu; K. Hirano; E. Tokunaga; N. Shibata (2015), "Organocatalyzed trifluormethylation of ketones and sulfonyl fluorides by fluoroform under a superbase system", ChemistryOpen 4 (5): 581–585, doi:10.1002/open.201500160, PMID 26491635 
  15. ↑ C. Kanazawa; K. Goto; M. Terada (2009), "Phosphazene base-catalyzed intramolecular cyclization for efficient synthesis of benzofurans via carbon-carbon bond formation", Chem. Commun. (35): 5248–5250, doi:10.1039/B913588J, PMID 19707635 
  16. ↑ B. Eßwein; M. Möller (1996), "Polymerisation von Ethylenoxid mit Alkyllithiumverbindungen und der Phosphazenbase "t Bu-P4"" (in German), Angew. Chem. 108 (6): 703–705, doi:10.1002/ange.19961080620, Bibcode: 1996AngCh.108..703E 
  17. ↑ P.C. Hupfield; R.G. Taylor (1999), "Ring-opening polymerisation of siloxanes using phosphazene base catalysts", J. Inorg. Organomet. Polym. Mater. 9 (1): 17–34, doi:10.1023/A:1021429320083 



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