Dimethyl-A- trimethylsilyl ethanamine

The product obtained from the above procedure is pure enough for most applications, but it should be redistilled through a fractionation column, and 

Submitted by ROBIN J. TERJESON, JO ANN CANICH, and GARY L. CARD Checked by MARK R. COLSMAN/ MARK A. UREMOVICH/ and STEVEN H, 

It is known that the introduction of SF groups into molecular systems can bring about significant changes in their physical, chemical, and biological 

The two-step procedure described here represents a convenient, facile synthesis that produces SF jC CH in high yields.  

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