Potassium thioacetate is used for palladium mediated coupling with aryl halides and triflates leading to S-arylthioacetates and derivatives. It is also used as a reagent in the conversion of halides to thiols.
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Applications
Potassium thioacetate is used for palladium mediated coupling with aryl halides and triflates leading to S-arylthioacetates and derivatives. It is also used as a reagent in the conversion of halides to thiols.
Solubility
Soluble in water, methanol and some polar solvents. Insoluble in alkanes, ethers and most nonpolar solvents.
Notes
Air sensitive. Hygroscopic. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong acids.
RUO – Research Use Only
General References:
- Reagent for the conversion of halides and sulfonates to thiols via the thiol acetates, thus avoiding the problem of sulfide formation: J. Chem. Soc., 579 (1950).
- Ortega, P.; Gómez, R.; de la Mata, F. J. Thiol ended carbosilane dendrimers. A multivalent platform for the binding of molecules of biological interest. Tetrahedron Lett. 2015, 56 (38), 5299-5302.
- Zhao, J.; Wang, C.; Zhao, P.; Wen, X.; Lin, C. Bioreducible dextran-polyethylenimine conjugates regulate transgene expression distribution in vivo. J. Mater. Chem. B 2015, 3 (8), 1529-1536.