HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34732Erstellt: 24. Oktober 2026
1-(Thiophen-3-yl)ethanone → Oxo(thiophen-3-yl)acetaldehyde
https://huagongshe.com/de/reaction/34732
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-(Thiophen-3-yl)ethanone | HCID 15116 | — |
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Oxo(thiophen-3-yl)acetaldehyde | HCID 249986 | — |
Reaktionsschritte
3-Acetylthiophene (20.0 g., 0.159 mol) and SeO2 (19.4 g., 0.175 mol) were dissolved 100 ml. dioxane and 8 ml. H2O by warming to 35°, then heated at reflux 16 hours. The reaction mixture was cooled, filtered and the filtrate stripped to a sludge (the hydrate of title product in crude form). The latter was distilled at reduced pressure to yield title product contaminated with about 10% starting material, 8.53 g.; tlc (5:3 hexane:ethyl acetate) Rf 0.27 (title product) and 0.59 (3-acetylthiophene). The latter was chromatographed on silica gel with 5:3 hexane:ethyl acetate is eluant. Clean product fractions were combined stripped to a solid, triturated with hexane, filtered and the solids (5.60 g.) sublimed to yield purified title product, 3.20 g.; tlc Rf 0.27 as above; sublimation point 70°/1 mm; ms: parent 141, base 111.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04762921 |
|---|
| Quelldatensatz | uspto-grants-1988_08 |
|---|
| ORD ID | ord-e0bc3c474aa34752b1b82f750db34eec |
|---|
| Quellennotiz | uspto-grants-1988_08 |
|---|