NEW SYNTHESIS OF FLUORINE-18-LABELED 6-FLUORO-L-DOPA BY CLEAVING THE CARBON-SILICON BOND WITH FLUORINE

  • 1 January 1985
    • journal article
    • research article
    • Vol. 26  (11) , 1314-1318
Abstract
A new synthesis of 3,4-dihydroxy-6-[18F]fluoro-L-phenylalanine using 6-trimethylsilyl-3,4-dimethoxy-L-dopa-ethylester as a fluorination substrate is described. The silane is prepared from the corresponding bromo compound by reacting the latter with magnesium and trimethylsilyl chloride. Reaction of the saline with [18F]F2 (0.5% F2 in neon) in a mixture of freon-11/CCl4 (1:1) kept in a dry ice bath, subsequent hydrolysis with concentrated HBr in a bath at 140.degree. C, and simple chromatographic purification.dag. yielded 18F-labeled 6-fluoro-L-dopa. A radiochemical yield of about 8% was achieved at the end of the 1-hr synthesis. The specific activity at the end of the synthesis was about 680 mCi/mmol after a 30-min irradiation.