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Suzuki-Miyaura Coupling in a Box

Product No. 802271


Compound Catalog No. Equivalents MW Density Amount mmol
Kit Components
Pd(dtbpf)Cl2 701602 0.026 651.75   9 mg 0.013
Triethylamine T0886 3.3 101.19 0.726 0.23 mL 1.65
TPGS-750-M 733857     1.002 1.0 mL  
User Supplied
Aryl bromide [ArBr]   1.0       0.5
Arylboronic acid [ArB(OH)2]   1.0-2.0       0.5-1.0


Please consult the Safety Data Sheet for information regarding hazards and safe handling practices.


  1. Add the aryl bromide (0.5 mmol) and the arylboronic acid (0.5-1.0 mmol) into the provided 5-mL reaction vial containing a stir bar and preloaded catalyst Pd(dtbpf)Cl2 (9 mg, 0.013 mmol) under N2.
  2. Replace the solid top cap with the provided septum top cap and connect with N2 bubbler through a needle.
  3. Transfer the provided TPGS-750-M/H2O (1.0 mL; 2 wt %) solution and Et3N (0.23 mL, 1.65 mmol) into the reaction vial using the provided syringe.
  4. Turn on the stirrer and stir the resulting mixture vigorously at room temperature until the reaction is complete (monitored by TLC, GC, LC, etc.).
  5. After completion, dilute the reaction mixture with 1-3 mL of EtOAc (or i-PrOAc) followed by gently stir for 2 minutes and then filter the entire mixture through a bed of silica gel plug (1 inch) on a sintered glass Buchner funnel (30 mm diameter).
  6. Wash the silica gel bed with an additional 1 mL of EtOAc (or i-PrOAc) and collect all of the coupled material.
  7. Remove all of the volatiles in vacuo and purify the crude material by flash column chromatography on silica gel.

More information on the research from the Lipshutz Group can be found in the Professor Product Portal.  

Additional information on TPGS-750-M: Second Generation Amphiphile for Organometallic Chemistry in Water at Room Temperature can be found in the Technology Spotlight section of our website.




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