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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587267Generated: November 3, 2026

1-Butanol → 2-(4-Hexylphenyl)-5-[4-(3-trimethylsilylpropoxy)phenyl]-1,3-thiazole

https://huagongshe.com/reaction/1587267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 19757554HCID 19757554—
Reactant4-{2-(4-Hexylphenyl)thiazole-5-yl}phenolHCID 23354762—
SolventWaterHCID 962—
Product2-(4-Hexylphenyl)-5-[4-(3-trimethylsilylpropoxy)phenyl]-1,3-thiazoleHCID 1975757370.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

0.34 g (1.0 mM) of 2-(4-hexylphenyl)-5-(4-hydroxyphenyl)-1,3-thiazole, 0.07 g of 85%-KOH and 12 ml of n-butanol were mixed. To the mixture, 0.29 g (1.0 mM) of 3-(trimethylsilyl)propyl p-toluenesulfonate was added dropwise under stirring at 100° C., followed by further stirring for 9 hours at 100° C. After the reaction, the reaction mixture was poured into water and extracted with ethyl acetate, followed by washing with water and drying with anhydrous magnesium sulfate. The magnesium sulfate in the resultant mixture was filtered off and the filtrate was condensed into a solid, followed by purification by silica gel column chromatography (eluent: toluene) and recrystallization from a mixture solvent (ethanol/ethyl acetate) to obtain 0.32 g of 2-(4-hexylphenyl)-5-[4-(3-trimethylsilylpropoxy)phenyl]-1,3-thiazole (Yield: 70.8%). ##STR81##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217645
Source datasetuspto-grants-1993_06
ORD IDord-3d4044e875fc41a684e5547f6f926eff
Source noteuspto-grants-1993_06