Abstract
The addition of 1-F-hexyl-2-bromoethanol and 2-F-hexyl-2-bromoethanol to aroxy-or alkoxysulfonyl isocyanates in anhydrous ether allowed the preparation of the corresponding brominated F-alkyl carbamates. In the case of 1-F-hexyl-2-bromoethanol, the easy cyclization of carbamates to F-alkyl oxazolidin-2-ones was achieved by the action of triethylamine in refluxing acetone.