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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039148Generated: October 25, 2026

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

https://huagongshe.com/reaction/1039148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Methoxy-phenyl)-2-methyl-thiazoleHCID 768765—
Reactant(6-Bromohexyloxy)-tert-butyldimethylsilaneHCID 4260352—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
SolventSodium chloride; waterHCID 57417360—
Product2-[7-(Tert-butyldimethylsilanyloxy)heptyl]-4-(4-methoxyphenyl)thiazoleHCID 6848993061.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552039B2
Source datasetuspto-grants-2013_10
ORD IDord-43b4714b1e834389a98d280abefa4705
Source noteuspto-grants-2013_10