Tri-tert-butylphosphonium tetrafluoroborate
ALDRICH/578940 - 97%
Synonym: TTBP ยท HBF4; [(t-Bu)3PH]BF4
CAS Number: 131274-22-1
Empirical Formula (Hill Notation): C12H28BF4P
Molecular Weight: 290.13
MDL Number: MFCD04039975
Linear Formula: [[(CH3)3C]3PH]BF4
Product Type: Chemical
| assay | 97% |
| form | solid |
| functional group | phosphine |
| InChI | 1S/C12H27P.BF4/c1-10(2,3) |
| InChI key | YTJUCJAUJCXFTN-UHFFFAOYSA |
| mp | 261 °C (lit.) |
| Quality Level | 100 ![]() |
| reaction suitability | reaction type: Cross Couplings |
| reagent type: ligand reaction type: Addition Reactions |
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| reagent type: ligand reaction type: Buchwald-Hartwig Cross Coupling Reaction |
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| reagent type: ligand reaction type: Carbonylations |
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| reagent type: ligand reaction type: Heck Reaction |
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| reagent type: ligand reaction type: Negishi Coupling |
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| reagent type: ligand reaction type: Sonogashira Coupling |
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| reagent type: ligand reaction type: Stille Coupling |
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| reagent type: ligand reaction type: Suzuki-Miyaura Coupling |
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| SMILES string | F[B-](F)(F)F.CC(C)(C)[PH+ |
| Application: | Hindered Phosphine salt employed with a Pd(0)-15-membered, triolefinic, macrocyle in Suzuki cross-coupling reactions of aryl bromides and chlorides. Also used in Heck coupling of non-activated vinyl tosylates with electron deficient olefins. |
| Application: | Ligand used in the Pd-catalyzed enantioselective α−arylation of N-boc-pyrrolidine. |
| Packaging: | 1, 5, 100 g in glass bottle |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | 97% |
| mp | 261 °C (lit.) |
| UNSPSC | 12352101 |

