ChemicalBook CAS DataBase List 4-Fluoro-1,1'-biphenyl

4-Fluoro-1,1'-biphenyl synthesis

14synthesis methods

Product Name:4-Fluoro-1,1'-biphenyl
CAS Number:324-74-3
Molecular formula:C12H9F
Molecular Weight:172.2

352-33-0
204 suppliers
$9.00/1g

(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)BENZENE

5123-13-7
122 suppliers
$22.00/5g

324-74-3
200 suppliers
$15.00/1g

Yield:324-74-3 99%

Reaction Conditions:

with potassium phosphate tribasic hydrate;Ni^IICl(1-naphthyl)(tricyclohexylphosphine)₂;tricyclohexylphosphine in tetrahydrofuran at 23; for 1 h;Inert atmosphere;Glovebox;Sealed tube;Suzuki-Miyaura Coupling;

Steps:

Cross-Coupling of ortho-, meta-, and para-Substituted, Electron-Rich and Electron-Deficient Aryl Halides and Aryl Mesylates with Aryl Neopentylglycolboronates Catalyzed by NiIICl(1-naph-thyl)(PCy3)2/PCy3 in Anhydrous THF at 23 °C; General Procedure 2

General procedure: Cross-Coupling of ortho-, meta-, and para-Substituted, Electron-Rich and Electron-Deficient Aryl Halides and Aryl Mesylates with Aryl Neopentylglycolboronates Catalyzed by NiIICl(1-naph-thyl)(PCy3)2/PCy3 in Anhydrous THF at 23 °C; General Procedure 2In an oven-dried test tube charged with a Teflon coated stirring barwere added aryl halide or aryl mesylate (0.3 mmol), aryl neopentyl-glycolboronates (0.315 mmol), K3PO4(H2O)3.2 (191.00 ± 1.00 mg, 0.9mmol), and NiIICl(1-naphthyl)(PCy3)2 (11.73 ± 0.0510 mg, 0.015mmol, 5% catalyst loading). The test tube was brought into a N2 filledglove box (moisture level <2 ppm) through three degassing cycles andPCy3 (8.4 mg, 0.03 mmol, 10% loading) ligand was added. Distilled sol-vent (1 mL) was added inside the glove box and the test tube wassealed by a rubber septum and left stirring at 23 °C. A sample was tak-en by syringe and transferred outside the glove box. The sample wasdiluted by distilled THF (0.2 mL) and filtered through a short columnof Al2O3. The filtrate was concentrated and the GC analysis was car-ried out. The reaction mixture was diluted with CH2Cl2 (2 mL), filteredthrough a layer of Al2O3, and washed with CH2Cl2 (3 1 mL). The fil-trate was collected and concentrated under vacuum. The crude prod-uct was purified by column chromatography on silica gel with EtO-Ac/hexane mixture as eluent. The reductive elimination side-productwas also isolated and characterized.

References:

Malineni, Jagadeesh;Jezorek, Ryan L.;Zhang, Na;Percec, Virgil [Synthesis,2016,vol. 48,# 17,art. no. SS-2016-C0279-ST,p. 2795 - 2807] Location in patent:supporting information

371-14-2 Synthesis