SummaryCarbon-11 labelled befloxatone ((5R)-5-(methoxymethyl)-3-[4-[(3R)-4,4,4-trifluoro-3-hydroxybutoxy]phenyl]-2-oxazolidinone) is a reversible and selective monoamine oxidase-A (MAO-A) inhibitor and appears to be a new potent PET tracer for the in vivo imaging of MAO-A density. In this paper, the radiosynthesis of befloxatone was investigated and orientated towards the preparation of multi milliCuries of radiotracer. Typically, using no-carrieradded [11 C]phosgene, 150-300 mCi (5.55-11.10 GBq) of [ 11 C]befloxatone was obtained within 20 min of radiosynthesis (including HPLC purification) with specific radioactivities ranging from 500 to 2000 mCi/mmol (18.5-74.0 GBq/ mmol). The high efficiency of these radiosyntheses allows for multi-injection protocols and kinetic approaches for absolute quantification of the tracer.