During natural behavior, an action often needs to be suddenly stopped in response to unexpected sensory input - referred to as reactive stopping. Reactive stopping has been mostly investigated in humans, which led to hypotheses about the involvement of different brain structures, in particular the hyperdirect pathway. Here, we directly investigate the contribution and interaction of two key regions of the hyperdirect pathway, the orbitofrontal cortex (OFC) and subthalamic nucleus (STN), using dual-area, multi-electrode recordings in male rats performing a stop-signal task. In this task rats have to initiate movement to a go-signal, and occasionally stop their movement to the go-signal side after a stop-signal, presented at various stop-signal delays.Both the OFC and STN show near-simultaneous field potential reductions in the beta frequency range (12-30Hz) compared to the period preceding the go-signal and the movement period. These transient reductions (∼200 ms) only happen during reactive stopping, which is when the stop-signal was received after action initiation, and are well-timed after stop-signal onset and before the estimated time of stopping. Phase synchronization analysis also showed a transient attenuation of synchronization between the OFC and STN in the beta range during reactive stopping.The present results provide the first direct quantification of local neural oscillatory activity in the OFC and STN and interareal synchronization specifically timed during reactive stopping.Significance Statement Different studies observed increases in oscillatory beta activity and suggested increased synchronization between the orbitofrontal cortex (OFC) and subthalamic nucleus (STN) during reactive stopping. However, there has been inconsistency in the timing of beta modulations, and no study has yet investigated phase synchronization during stopping in both the OFC and STN with anatomical and temporal precision. Using dual-area recordings during a stopping task, we observed substantial decreases in beta power in both the OFC and STN at the time of stopping, alongside a decrease in beta phase synchronization. Rather than increased beta-band activity, the OFC and STN appear to facilitate stopping through local and inter-areal desynchronization. This may enable functionally specific neuronal activity to selectively inhibit motor behavior downstream.