The present invention relates to a preparation method of an organofluorine compound, and more particularly to a preparation method of 2,3,3,3-tetrafluoropropene, wherein the method is based on 2,3-dichloro-1,1,1-trifluoropropane as a
raw material, and under the
joint action of a Lewis acid catalyst and a fluorinating agent, 2-chloro-1,1,1,2-tetrafluoropropane is reacted to obtain 2,3,3,3-tetrafluoropropene, and finally the 2-chloro-1,1,1,2-tetrafluoropropene prepared is reacted with an alkali, and
hydrogen chloride is removed to obtain 2,3,3,3-tetrafluoropropene. The method in this application has the advantages that
reaction conditions are mild and selectivity is high, so that the preparation efficiency of 2,3,3,3-tetrafluoropropene can be significantly improved during the reaction. In addition, the separation and collection difficulty of product can also be effectively reduced by the method in the present invention, and the manufacturing cost of 2,3,3,3-tetrafluoropropene is reduced.