Photoredox Cross-Coupling HCK1009-01-004

2 sets of reaction conditions with iridium catalyst Ir(dF-CF₃–ppy)₂(dtbbpy)PF₆, 4 Ni ligands dtbbpy, bphen, (MeO)₂bpy and biox, and 8 bases Cs₂CO₃, K₃PO₄, K₂HPO₄, KOH, Li₂CO₃, K₂CO₃, DABCO and DBU. 32 reaction vials total.

This kit requires EvoluChem™ PhotoRedOx Box –HCK1006-01-016and EvoluChem™ Light Source 18W-450 nm –HCK1012-01-002as well asSyringe, decapper and reaction block included in the EvoluChem™ Starter Kit (HCK1006-01-001)

The typical protocol is performed at 0.05 mol/l using a solution containing two coupling components. Each sealed reaction vial contains 0.1 μmol of photocatalyst, 0.5 μmol Ni catalyst, 0.5 μmol ligand and 15 of μmol base (for all bases except for DBU conditions, base is added separately and shipped in a separate vial).The Ir/Ni photoredox kit contains 2 sets of vials allowing the screening of two different solvents. Sparging reaction solvents with nitrogen or argon while transferring reagents is important to achieve highest conversions of product. See protocol diagram for instructions.The vial holder shipped with the kit can be placed directly on the photochemistry device.

Protocol at 100 μl volume reaction condition

• Prepare the required volume of substrate solution at 0.05 mol/L containing both coupling substrates. For example, 2600 μl solution for 24 reaction conditions (200 μl extra to compensate for evaporation).
• Degas substrate solution with subsurface sparging via N2 or Ar line with exit needle for 5 minutes.
• Using a clean and dry syringe, add 100 μl of the substrate solution to each reaction vial (excluding vials containing DBU for now).
• Add 400 ul of substrate solution to vial containing DBU base vial. Repeat degas of solution.****
• Add 100 ul of substrate/DBU solution to each DBU reaction vial (4x)
• Repeat steps 2 and 5 for each substrate solvent mixture.
• Stir the reaction vials for 5 minutes prior to turning on the light to allow catalysts to fully dissolve (some bases will remain insoluble).
• Turn on lamp and stir vials for 18 to 24 hours (or longer if necessary). Be sure to plug in fan to maintain RT.
• Upon completion of reaction, remove the vial caps using a decapper.
• Prepare analytical sample for each reaction condition with 5 μl sample diluted into 200 μl in either DMSO or water/acetonitrile 50/50. Alternatively, reaction solvent can be evaporated in vacuo and crude mixture diluted in water/acetonitrile prior to preparation of analytical sample.
• Analyze resulting analytical samples by LC/MS.

***Alternatively, 2.24 μl of DBU can be added to each of the DBU reactions separately using 10 ul Hamilton Syringe (not provided) instead of premixing substrate solutions and DBU base. In this case, first add 100 μl substrate solution to DBU reaction vials, followed by addition of 2.24 μl DBU and proceed to step 6.