The invention discloses a vitamin K3 drug intermediate 2-menaquinone synthesis method, which comprises: adding 1,4-dihydroxy-2-methyl naphthalene and a potassium chloride solution in a reaction container, increasing the temperature of the solution, controlling the stirring speed, adding an acetylacetone solution, carrying out a reaction, adding thulium oxide in batches, increasing the temperatureof the solution, carrying out a reaction for 60-90 min, adding a potassium sulfate solution, reducing the temperature to 10-16 DEG C, carrying out standing layering, adding an oxalic acid solution, adjusting the pH value to 5-6, washing with a 3-chloro-1-propanol solution, washing with a chlorohexane solution, re-crystallizing in a sulfuryl chloride solution, and dehydrating with a dehydrating agent to obtain the finished product 2-menaquinone.