ChemicalBook--->CAS DataBase List--->131274-22-1

131274-22-1

131274-22-1 Structure

131274-22-1 Structure
IdentificationMore
[Name]

Tri-tert-butylphosphine tetrafluoroborate
[CAS]

131274-22-1
[Synonyms]

TRI-(T-BUTYL)PHOSPHONIUM HYDROGEN HBF4 SALT
TRI-T-BUTYLPHOSPHONIUM TETRAFLUOROBORATE
TRI-TERT-BUTYLPHOSPHINE TETRAFLUOROBORATE
TRI-TERT-BUTYLPHOSPHINE TETRAFLUOROBORIC ACID ADDUCT
TRI-TERT-BUTYLPHOSPHONIUM TETRAFLUOROBORATE
TRI-TERT-BUTYLPHOSPHINE TETRAFLUOROBORA&
Tri-t-butylphosphoniumtetrafluoroborate,99%
fluoroboric acid tri-tert-butylphosphine adduct
tri-tert-butylphosphine fluoroboric acid adduct
Tri-tert-butylphosphonium tetrafluoroborate, 97+%
Tri-tert-butylphosphonium tetrafluoroborate,99%
[EINECS(EC#)]

672-603-2
[Molecular Formula]

C12H27BF4P-
[MDL Number]

MFCD07189501
[Molecular Weight]

289.12
[MOL File]

131274-22-1.mol
Chemical PropertiesBack Directory
[Appearance]

white to light yellow crystal powde
[Melting point ]

261 °C(lit.)
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

Chloroform (Slightly), Dichloromethane (Slightly), Methanol (Slightly)
[form ]

Crystals and Chunks
[color ]

White
[Water Solubility ]

Soluble in methylene chloride and chloroform. Slightly soluble in terahydro furan. Insoluble in hexane, toluene and water.
[Sensitive ]

Hygroscopic
[BRN ]

8813613
[InChI]

InChI=1S/C12H28P.BF4/c1-10(2,3)13(11(4,5)6)12(7,8)9;2-1(3,4)5/h13H,1-9H3;/q2*-1
[InChIKey]

YSTLBJVHZMEEAC-UHFFFAOYSA-N
[SMILES]

[P-](C(C)(C)C)(C(C)(C)C)C(C)(C)C.[B-](F)(F)(F)F
[CAS DataBase Reference]

131274-22-1(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[RIDADR ]

UN 1759 8/PG III
[WGK Germany ]

3
[TSCA ]

No
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

29319090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Ethyl acetate-->Tetrahydrofuran-->Hexane-->Magnesium-->Phosphorus trichloride-->Fluoroboric acid-->tert-Butyllithium-->2-Chloro-2-methylpropane-->2-Bromo-2-methylpropane
Hazard InformationBack Directory
[Chemical Properties]

white to light yellow crystal powde
[Uses]

suzuki reaction
[Application]

Tri-tert-butylphosphonium tetrafluoroborate is a ligand used in the palladium-catalyzed enantioselective alfa-arylation of N-boc-pyrrolidine. It is also used with a palladium(0)-15-membered, triolefinic, macrocyle in Suzuki cross-coupling reactions of aryl bromides and chlorides. Further, it is used in the Heck coupling of vinyl tosylates with olefins.
[Preparation]

Addition of HBF4 to a solution of tri-tert-butylphosphine in methylene chloride. Separation of the organic layer and removal of the solvent gives analytically pure Tri-tert-butylphosphine tetrafluoroborate.
[storage]

Tri-tert-butylphosphine tetrafluoroborate is indefinitely stable as a solid and in solution and requires no special handling. This compound is considered non-hazardous. Protection from oxygen is required in the presence of the base, as the highly air-sensitive tri-tert-butylphosphine will be formed.
Questions And AnswerBack Directory
[Reaction]

  1. Air-stable, non-pyrophoric precursor of the Tri-t-butylphosphine ligand which is used in a variety of catalytic processes.
  2. Ligand for Suzuki cross-couplings.
  3. Ligand for Heck Reactions.
  4. Ligand for Stille Cross-couplings.
  5. Ligand for α-Arylation and vinylation of arylmandelic acid derivatives.
  6. Ligand for direct arylation of hetercycles
  7. Synthesis of benzocyclobutenes by C-H activation.
  8. Cross-coupling of Grignard reagents and aryl bromides.
  9. Palladium catalyzed annulation of haloanilines.
  10. Palladium-Catalyzed Acylation.
  11. Palladium Catalyzed Carbonylative Heck Reaction.
  12. Palladium-catalyzed aminosulfonylation.
  13. Palladium-catalyzed intramolecular C–O bond formation.
  14. Ruthenium-catalyzed cross-coupling of aldehydes with arylboronic acid.
Reactions of 131274-22-1_1
Reactions of 131274-22-1_2
Reactions of 131274-22-1_3
Reactions of 131274-22-1_4
Spectrum DetailBack Directory
[Spectrum Detail]

Tri-tert-butylphosphine tetrafluoroborate(131274-22-1)1HNMR
Tri-tert-butylphosphine tetrafluoroborate(131274-22-1)31PNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Tri-tert-butylphosphonium tetrafluoroborate, 97+%(131274-22-1)
[Alfa Aesar]

Tri-tert-butylphosphonium tetrafluoroborate, 97%(131274-22-1)
[Sigma Aldrich]

131274-22-1(sigmaaldrich)
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