HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Thiophen-3-yl)ethanone → 1-(5-Thiazolyl)-1-(3-thienyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Thiophen-3-yl)ethanone | HCID 15116 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Trimethylsilylthiazole | HCID 588453 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(5-Thiazolyl)-1-(3-thienyl)ethanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05607956 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-cac5ce3fe56c4f4ca6d36c22ccce9988 |
| Source note | uspto-grants-1997_03 |