Methanol and concentrated sulphuric acid are taken as
solvent and 2-chloric
mandelic acid is taken as
raw material for
esterification reaction,
sodium hydroxide is added to be neutral after full reaction, reducing reaction is carried out with
sodium borohydride, diluted
hydrochloric acid is used for
neutralization and water is added for
dilution,
distillation and extraction by 1, 2-
dichloroethane are carried out to obtain 1-2-(2-chlorphenyl)-1, 2-
ethylene glycol, then
triethylamine and mesyl
chloride are added into the 1-2-(2-chlorphenyl)-1, 2-
ethylene glycol for
esterification reaction, and then diluted
hydrochloric acid,
sodium bicarbonate and drinking water are respectively used for washing, reduced pressure
distillation is carried out to remove
solvent, so as to obtain sticky
grease,
ethyl acetate is added at the temperature below 77 DEG C for
dissolution, heating is carried out until refluxing, temperature reduction,
crystallization,
centrifugation and
drying are carried out, thus obtaining yellow
solid 1-(2-chlorphenyl)-1, 2-glycol dimethyl sulphonate. Then dimethyl sulphoxide and
potassium hydroxide are taken as raw materials, mixed liquid of 1-imidazoly
acetonitrile, carbon disulphide and dimethyl sulphoxide is dropwise added for
condensation reaction, mixed liquid of dimethyl sulphoxide and 1-(2-chlorphenyl)-1, 2-glycol dimethyl sulphonate is dropwise added for ring formation reaction, and ice analysis, extraction by
ethyl acetate and reduce pressure
distillation are carried out, thus obtaining E / Z-alpha-[4-(2-chlorphenyl)-1, 3-
dithiolane-2-
subunit]-1H-imidazolyl
acetonitrile. The E / Z-alpha-[4-(2-chlorphenyl)-1, 3-
dithiolane-2-
subunit]-1H-imidazolyl
acetonitrile is separated by silicagel column and then added with
active carbon, distillation is carried out to remove most
solvent,
hot pressing filtering, temperature reduction,
crystallization,
centrifugation and
drying are carried out, thus obtaining almost white or white lanoconazole
powder solid.