2-Di-tert-butylphosphino-2',4',6'-triisopropylbiphenyl

• Effective ligand for the Pd-catalyzed arylation of pyrazoles, indazoles and amino heterocycles.
• Ligand used in the Pd-catalyzed synthesis of phenols from aryl halides and KOH.
• Ligand used in the Pd-catalyzed of benzoic acids from aryl halides and CO2.
• Ligand used in the Pd-catalyzed trifluoromethylation of vinyl sulfonates.
• Ligand used in the Pd-catalyzed arylation of nitroacetates.
• Ligand used in the Pd-catalyzed Suzuki−Miyaura cross-coupling of allylboronates and aryl halides.
• Ligand used in the Pd-catalyzed cyanation of (hetero)arylchlorides and bromides.
• Ligand used in the Pd-catalyzed C–N cross coupling of sulfinamides and aryl halides.
• Ligand used in the Pd-catalyzed arylation of cyanamides. 

• Palladium-catalyzed Tsuji-Trost substitution and cross-coupling of benzylic fluorides.
• Palladium-catalyzed C-N cross-coupling of sulfinamides and aryl halides.
• Palladium-catalyzed rapid methoxylation and deuteriomethoxylation of bromo-chalcones.

13716-10-4

694-80-4

21524-34-5

564483-19-8

1. In a 1L three-necked flask, 32.5 g of 2-bromo-1,3,5-triisopropylbenzene, 5.6 g of magnesium shavings, and 300 mL of anhydrous tetrahydrofuran (THF) were added to prepare a Grignard reagent. 2. Under stirring, 20 g of 2-bromochlorobenzene was slowly added dropwise to the above solution to form 2,4,6-triisopropyl-2'-bromodiphenyl Grignard reagent, and the reaction was refluxed for 2 hours. 3. After completion of the reaction, cooled to room temperature, 2.4 g of tetrakis(triphenylphosphine)palladium was added as a catalyst and stirred for 30 minutes. 4. At room temperature, 18.8 g of di-tert-butylphosphonium chloride was slowly added dropwise to the reaction mixture and the reaction was continued at reflux for 5 hours. 5. The reaction mixture was cooled in an ice water bath and 200 mL of saturated aqueous ammonium chloride solution was slowly added dropwise to quench the reaction. 6. The organic phase was separated and crystallized by addition of methanol and filtered to afford 41.7 g of the white solid product 2-di-tert-butylphosphino-2',4',6'-triisopropylbiphenyl in 94% yield.