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Sodium tetraphenylboron (STPB)

  • Product Name: Sodium tetraphenylboron (STPB)
  • CAS: 143-66-8
  • Purity:
  • Appearance: white powder

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Factory supply Sodium tetraphenylboron (STPB) 143-66-8 with sufficient stock and high standard

  • Molecular Formula:C24H20BNa
  • Molecular Weight:342.224
  • Appearance/Colour:white powder 
  • Melting Point:300 °C 
  • PSA:0.00000 
  • Density:1.15 g/cm3 
  • LogP:3.06400 

Sodium tetraphenylboron(Cas 143-66-8) Usage

General Description

Sodium tetraphenylborate (Ph4BNa) undergoes rhodium-catalyzed addition reactions with N-phenylsulfonyl aldimines to afford R(Ph)CHNHSO2Ph.

Purification Methods

Dissolve the borate in dry MeOH and add dry Et2O. Collect the solid and dry it in a vacuum at 80o/2mm for 4hours. It can also be extracted (Soxhlet) using CHCl3, and it crystallises from CHCl3 as snow-white needles. It is freely soluble in H2O, Me2CO but insoluble in pet ether and Et2O. An aqueous solution has pH  5 and can be stored for days at 25 or lower, and for 5 days at 45o without deterioration. Its solubility in polar solvents increases with decrease in temperature [Wittig & Raff Justus Liebigs Ann Chem 573 204 1950]. The salt can also be recrystallised from acetone/hexane or CHCl3, or from Et2O/cyclohexane (3:2) by warming the solution to precipitate the compound. Dry it in a vacuum at 80o. It dissolves in Me2CO at 50-60o to give a clear solution. After standing at this temperature for 10minutes the mixture is filtered rapidly through a pre-heated Büchner funnel, cooled and the crystals are collected and dried in a vacuum desiccator at room temperature for 3days [Abraham et al. J Chem Soc, Faraday Trans 1 80 489 1984]. If the product gives a turbid aqueous solution, the turbidity can be removed by treating with freshly prepared alumina gel and filtering. [Beilstein 16 IV 1624.]

InChI:InChI:1S/C24H20B.Na/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24;/h1-20H;/q-1;+1

143-66-8 Relevant articles

Base-free palladium-catalyzed cross-coupling of arylsulfonium salts with sodium tetraarylborates

Osuka, Atsuhiro,Vasu, Dhananjayan,Yorimitsu, Hideki

, p. 3286 - 3291 (2020/10/20)

Palladium-catalyzed cross-coupling react...

Palladium-Assisted "Aromatic Metamorphosis" of Dibenzothiophenes into Triphenylenes

Vasu, Dhananjayan,Yorimitsu, Hideki,Osuka, Atsuhiro

supporting information, p. 7162 - 7166 (2015/06/08)

Abstract Two new palladium-catalyzed rea...

Ligand-free, atom-efficient Suzuki-Miyaura type cross-coupling reactions at room temperature

Zhou, Wen-Jun,Wang, Ke-Hu,Wang, Jin-Xian,Gao, Zhi-Rong

experimental part, p. 7633 - 7641 (2010/12/19)

The atom-efficient cross-coupling reacti...

143-66-8 Process route

sodium tetrafluoroborate
13755-29-8

sodium tetrafluoroborate

bromobenzene
108-86-1,52753-63-6

bromobenzene

sodium tetraphenyl borate
143-66-8

sodium tetraphenyl borate

Conditions
Conditions Yield
With magnesium; In tetrahydrofuran; at 0 - 20 ℃; for 12h; Inert atmosphere;
sodium tetrafluoroborate
13755-29-8

sodium tetrafluoroborate

phenylmagnesium bromide
100-58-3

phenylmagnesium bromide

sodium tetraphenyl borate
143-66-8

sodium tetraphenyl borate

Conditions
Conditions Yield
In diethyl ether; heating on water bath;
With sodium chloride; In diethyl ether; water; 2 h stirring, addn. of reaction mixture to a satd. aq. NaCl soln.; extrn. the aq. layer with ether two times, evapn. in vac.; recrystn. in ether at 0°C;
In diethyl ether; heating on water bath;
With NaCl; In diethyl ether; water; 2 h stirring, addn. of reaction mixture to a satd. aq. NaCl soln.; extrn. the aq. layer with ether two times, evapn. in vac.; recrystn. in ether at 0°C;

143-66-8 Upstream products

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    triphenylborane

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    potassium tetraphenylborate

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    trifluoroborane diethyl ether

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    phenylmagnesium bromide

143-66-8 Downstream products

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    3-cyclohexyl-2-oxa-3-aza-[4.4.4]propell-3-enium; tetraphenylborate(1-)

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    2-Brom-1,1-dimethyl-propoxy(3H6)dimethylsulfonium-tetraphenylborat

  • 50592-81-9
    50592-81-9

    C24H20B(1-)*C9H15O4S(1+)

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