Organic catalyst 54010-75-2 high purity Organic catalyst
Product Name: | Zinc trifluoromethanesulfonate |
Synonyms: | Zinc trifluoromethylsulfonate;Zn(OTf)2;Bis(trifluoromethanesulfonato)zinc;trifluoro-methanesulfonicacizincsalt;Trifluoromethane sulfonic acid zinc;Zinc trifluoromethanesulfonate, min. 98%;ZINC TRIFLUOROMETHANESULFONATE;ZINC TRIFLUOROMETHANESULPHONATE |
CAS: | 54010-75-2 |
MF: | C2F6O6S2Zn |
MW: | 363.53 |
EINECS: | 258-922-6 |
Product Categories: | metal triflate compounds;OTf&NTf series;Catalysts for Organic Synthesis;Classes of Metal Compounds;Homogeneous Catalysts;Other Metal;Metal Triflates;Synthetic Organic Chemistry;Transition Metal Compounds;Zn (Zinc) Compounds;triflate |
Uses | Zinc trifluoromethanesulfonate acts as a catalyst for the preparation of dithioketals. It is used as a Lewis acid catalyst in silylation reactions. It is also used as a catalyst for greener amine synthesis by reductive amination with hydrogen gas. |
Synthesis | Triflic acid (0.056mol) was added dropwise to a suspension of zinc carbonate (0.02 mol)in dry methanol (20 ml) at room temperature. During the addition, CO2 was evolved. The mixture was stirred at 25°C for 20 minutes and refluxed for 2 h. The clear solution was cooled to 25°C and concentrated under reduced pressure. The resulting white powder was dried at 125°C for 2 h to afford Zinc trifluoromethanesulfonate (Zn(OTf)2 )(98% yield). |
Purification Methods | It should be dried at 125o for 2hours at 3mm before use. It is soluble in CH2Cl2 but insoluble in pet ether. [Corey & Shimoji Tetrahedron Lett 24 169 1983.] |
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