Straatmann M G, Welch M J
J Nucl Med. 1977 Feb;18(2):151-8.
A new fluorinating agent was developed by incorporation of 18F into diethylaminosulfur trifluoride (DAST), a reagent capable of replacing hydroxyl and carbonyl oxygen with fluorine. The DAST was synthesized using sulfur tetrafluoride and trimethylsilyldiethylamine in a freon-11 solvent at -78 degrees C and purified by reduced-pressure distillation. Labeling was then accomplished by exchange with anhydrous 18F-hydrofluoric acid, which caused more than 80% of the available activity to be incorporated into the DAST. Fluorine-18-labeled methyl fluoride, ethyl fluoride, and 2-fluoroethanol were prepared from methanol, ethanol, and ethylene glycol, with yields of 20%, 25%, and 12%, respectively.
通过将18F引入二乙氨基三氟化硫(DAST)开发出一种新型氟化剂,DAST是一种能够用氟取代羟基和羰基氧的试剂。在-78℃下于氟利昂-11溶剂中使用四氟化硫和三甲基硅基二乙胺合成DAST,并通过减压蒸馏进行纯化。然后通过与无水18F-氢氟酸交换来完成标记,这使得超过80%的可用活性被并入DAST中。由甲醇、乙醇和乙二醇分别制备出氟-18标记的氟甲烷、氟乙烷和2-氟乙醇,产率分别为20%、25%和12%。