Use of SF4 For The Synthesis of Fluorocarbons
In organic synthesis, SF4 is used to convert COH and C=O groups into CF and CF2 groups, respectively. Certain alcohols readily give the corresponding fluorocarbon. Ketones and aldehydes give geminal difluorides. The presence of protons alpha to the carbonyl leads to side reactions and diminished (30–40%) yield. Also diols can give cyclic sulfite esters, (RO)2SO. Carboxylic acids convert to trifluoromethyl derivatives. For example treatment of heptanoic acid with SF4 at 100-130 °C produces 1,1,1-trifluoroheptane. The coproducts from these fluorinations, including unreacted SF4 together with SOF2 and SO2, are toxic but can be neutralized by their treatment with aqueous KOH.
The use of SF4 is being superseded in recent years by the more conveniently handled diethylaminosulfur trifluoride, Et2NSF3, "DAST", where Et = CH3CH2. This reagent is prepared from SF4:
- SF4 + Me3SiNEt2 → Et2NSF3 + Me3SiF
Read more about this topic: Sulfur Tetrafluoride
Famous quotes containing the word synthesis:
“If in the opinion of the Tsars authors were to be the servants of the state, in the opinion of the radical critics writers were to be the servants of the masses. The two lines of thought were bound to meet and join forces when at last, in our times, a new kind of regime the synthesis of a Hegelian triad, combined the idea of the masses with the idea of the state.”
—Vladimir Nabokov (1899–1977)