Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975061Generated: October 26, 2026

1-(Thiophen-3-yl)ethanone → 1-(5-Thiazolyl)-1-(3-thienyl)ethanol

https://huagongshe.com/reaction/975061

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Thiophen-3-yl)ethanoneHCID 15116—
ReactantSodium BicarbonateHCID 516892—
Reactant2-TrimethylsilylthiazoleHCID 588453—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product1-(5-Thiazolyl)-1-(3-thienyl)ethanolHCID 18936319—

Reaction Steps

n-Butyllithium (2.5M solution in hexane, 5.6 ml) in diethylether (25 ml) was stirred at -70° C. under a nitrogen atmosphere and 2-trimethylsilylthiazole (2 g) in diethylether (25 ml) was added dropwise. After 30 minutes 3-acetylthiophene (1.93 g) in diethylether (25 ml) was added dropwise. After a further 45 minutes the mixture was allowed to warm to room temperature and then left to stir for a further 1 hour. Saturated aqueous sodium hydrogen carbonate was added and the organic layer was separated. The aqueous layer was extracted with diethylether. The organic layers were combined, washed, dried and evaporated and the residue was purified by flash chromatography to give the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607956
Source datasetuspto-grants-1997_03
ORD IDord-cac5ce3fe56c4f4ca6d36c22ccce9988
Source noteuspto-grants-1997_03