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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1039148Erstellt: 27. Oktober 2026

4-(4-Methoxy-phenyl)-2-methyl-thiazole → 2-[7-(Tert-butyldimethylsilanyloxy)heptyl]-4-(4-methoxyphenyl)thiazole

https://huagongshe.com/reaction/1039148

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(4-Methoxy-phenyl)-2-methyl-thiazoleHCID 768765—
Edukt(6-Bromohexyloxy)-tert-butyldimethylsilaneHCID 4260352—
EduktHCID 178418306HCID 178418306—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelAmmonium ChlorideHCID 25517—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt2-[7-(Tert-butyldimethylsilanyloxy)heptyl]-4-(4-methoxyphenyl)thiazoleHCID 6848993061,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Add a solution of tert-butyllithium (26.35 mmol, 15.5 mL, 1.7 M in hexanes) dropwise to a solution of 4-(4-methoxyphenyl)-2-methylthiazole (6.15 g, 29.9 mmol) in degassed anhydrous tetrahydrofuran (THF) (100 mL) at −78° C. under nitrogen and stir the solution for 45 minutes. To this solution, add a solution of (6-bromohexyloxy)-tert-butyldimethylsilane (7.20 g, 24.4 mmol) over 5 min and stir the mixture for 2 hours. Warm the mixture to 0° C., dilute with NH4Cl (200 mL) and brine (250 mL) and extract with methylene chloride (3×150 mL). Dry the combined organic extracts over magnesium sulfate and remove the solvent under reduced pressure. Purify the crude product by flash column chromatography on silica gel, eluting with hexanes/ethyl acetate (5:1), to provide 2-[7-(tert-butyldimethylsilanyloxy)heptyl]-4-(4-methoxyphenyl)thiazole (6.27 g, 50%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08552039B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-43b4714b1e834389a98d280abefa4705
Quellennotizuspto-grants-2013_10