Abstract: | 2-Hydroperfluoropropyl azide CF3CHFCF2N3, 1 , an inexpensive, readily available, and stable (easy to store) compound, is suggested as an effective fluorinating reagent for different classes of trivalent organophosphorus compounds in accordance with the general scheme R3P → R3PF2. Generally, the reactions are performed without solvent, the highly volatile CF3 CHFCN being the main by-product. The fluorination is usually an exothermic process, but slight heating is necessary in the case of alkyldifluorophosphites. The unusual Arbuzov rearrangement, accompanied by isomerization of an isobutyl or neopentyl group into a tert-group, ROPF2 → t-R′POF2, under the action of a catalytic amount of 1 , was observed. |