HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2807Erstellt: 24. Oktober 2026
Thiophene → 1-(4-Methyl-5-oxazolyl)-1-(2-thienyl)ethanol
https://huagongshe.com/de/reaction/2807
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Thiophene | HCID 8030 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 1-(4-Methyloxazol-5-yl)ethanone | HCID 11029839 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(4-Methyl-5-oxazolyl)-1-(2-thienyl)ethanol | HCID 18936327 | — |
Reaktionsschritte
Thiophene (3.36 g) in dry tetrahydrofuran (20 ml) was stirred and cooled to -40° C. under a dry nitrogen atmosphere and n-butyllithium (2.5M solution in hexane, 16 ml) was added dropwise. The mixture was allowed to warm to -20° C. and then after 1 hour was cooled to -70° C. 5-Acetyl-4-methyloxazole (5 g) in dry tetrahydrofuran (15 ml) was added dropwise. After a further 1 hour the mixture was allowed to warm the room temperature and was stirred for a further 2 hours. Aqueous sodium hydrogen carbonate was added and the mixture was extracted with diethylether. The material thus obtained was purified by flash chromatography to give the title compound. M.p. 84°-85° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05731335 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-0cd8b984bb7449ec9670db072ec4ad56 |
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| Quellennotiz | uspto-grants-1998_03 |
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