A kind of preparation method of pharmaceutical intermediate
An intermediate and pharmaceutical technology, applied in the field of chemical and pharmaceutical intermediates, to achieve the effects of cheap and easy-to-obtain raw materials, novel synthetic routes, and simple operations
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[0026] The present invention starts from the raw material (R)-epichlorohydrin, and provides a pharmaceutical intermediate (S)-1-[(4S,5R)-4-(2,2 - a preparation method of dimethyl-5E-propenyl-1,3-dioxol (1,3-dioxol)]-1-octanol (1), which comprises 8 steps of reaction in total.
[0027] (a) Preparation of (R)-1-chloro-5-trimethylsilyl-4-pentyn-2-alcohol:
[0028] Under anhydrous and oxygen-free conditions, dissolve trimethylsilylacetylene (5.82g, 0.06mol) in anhydrous tetrahydrofuran (250mL), add butyllithium (2.5M, 24mL, 0.06mol) dropwise at minus 78 degrees, and stir After 1 hour, add boron trifluoride diethyl ether (0.06mol), and after 10 minutes, add the raw material R-epichlorohydrin (4.85g, 0.05mol), keep the temperature for 2 hours, then raise the temperature to minus 30 degrees, and keep the reaction for 19 After 1 hour, TLC detected that the reaction of the raw materials was complete, adding saturated ammonium chloride to quench the reaction, distilling off the solvent...
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