The invention discloses a trifluoromethyl substituted continuous quaternary carbon center cyclopropane derivative and a synthetic method, belonging to the technical field of synthesis of medicine chemical industry. The synthetic method comprises the following steps: adding N-tosyl hydrazone, trifluoromethyl ketone, alkali, a phase transfer catalyst and a solvent into a reactor, carrying out reaction under stirring at 70 to 90 DEG C for 12 to 24 hours, after the reaction is completed, carrying out cooling to room temperature, filtering obtained reaction liquid, carrying out vacuum evaporation and removing the solvent so as to obtain a crude trifluoromethyl substituted continuous quaternary carbon center cyclopropane derivative, and carrying out purifying through column chromatography so as to obtain the trifluoromethyl substituted continuous quaternary carbon center cyclopropane derivative. The method provided by the invention avoids using a transition metal catalyst and uses non-toxic, cheap and easily-available raw materials; the reaction has good adaptability to functional groups and wide adaptability to a substrate, has high product yield and good non-reflect selectivity, can be enlarged to gram-grade scale production and synthesis, and is favorable for industrial production; meanwhile, the obtained trifluoromethyl substituted continuous quaternary carbon center cyclopropane derivative has extensive application in the fields of pesticides, medicines and materials.