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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1534611Erstellt: 26. Oktober 2026

tert-Butyldimethylsilyl chloride → 2-[1-(5-Tert-butyldimethylsilyloxy-3-(naphth-2-ylmethoxy)phenyl)-1-methoxypropyl]thiazole

https://huagongshe.com/reaction/1534611

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
EduktEthyl 5-hydroxy-3-(naphth-2-ylmethoxy)benzoateHCID 19773027—
EduktHCID 178461634HCID 178461634—
EduktHCID 178506781HCID 178506781—
Produkt2-[1-(5-Tert-butyldimethylsilyloxy-3-(naphth-2-ylmethoxy)phenyl)-1-methoxypropyl]thiazoleHCID 1977300642%

Reaktionsschritte

Ethyl 5-hydroxy-3-(naphth-2-ylmethoxy)benzoate, obtained from ethyl 3,5-dihydroxybenzoate and 2-bromomethylnaphthalene, was reacted with tert-butyldimethylsilyl chloride using the conditions described in the 1st paragraph of the portion of Example 6 which is concerned with the preparation of starting materials and the product so obtained was reacted in turn with thiazol-2-yl-lithium and ethylmagnesium iodide following the procedures described in the portion of Example 3 which is concerned with the preparation of starting materials. There was thus obtained the required starting material in 49% yield (from ethyl 5-hydroxy-3-(naphth-2-ylmethoxy)benzoate) as an oil. This starting material was methylated using the procedure described in Example 3 to give 2-[1-(5-tert-butyldimethylsilyloxy-3-(naphth-2-ylmethoxy)phenyl)-1-methoxypropyl]thiazole as an oil, in 42% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05089513
Quelldatensatzuspto-grants-1992_02
ORD IDord-a8cde654e8b74c47ae13f12277e3e504
Quellennotizuspto-grants-1992_02