HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1375031Erstellt: 26. Oktober 2026
p-Toluenesulfonic acid → 2-[3,4-dihydro-2H-pyrido[3,2-b]-1,4-oxazin-4-yl]acetaldehyde
https://huagongshe.com/reaction/1375031
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 3,4-dihydro-4-[(1,3-dioxolan-2-yl)methyl]-2H-pyrido[3,2-b]-1,4-oxazine | HCID 17963940 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-[3,4-dihydro-2H-pyrido[3,2-b]-1,4-oxazin-4-yl]acetaldehyde | HCID 17963972 | 86,3% |
Reaktionsschritte
A solution of 3,4-dihydro-4-[(1,3-dioxolan-2-yl)methyl]-2H-pyrido[3,2-b]-1,4-oxazine (0.13 g) in acetone (10 ml) and water (1 ml) was heated under reflux in the presence of p-toluenesulfonic acid (2.24 g) for 3 days. The mixture was concentrated in vacuo and the residue was poured into aqueous saturated sodium hydrogen carbonate solution. The water layer was extracted with ethyl acetate three times and the combined organic layers were dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel using a mixed solvent of methanol and dichloromethane (1:10) as an eluent. The fractions containing the objective compound were collected and evaporated under reduced pressure to give 2-[3,4-dihydro-2H-pyrido[3,2-b]-1,4-oxazin-4-yl]acetaldehyde (0.09 g) as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07166598B2 |
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| Quelldatensatz | uspto-grants-2007_01 |
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| ORD ID | ord-c8c5958e1c38402fb281b123c9096c6c |
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| Quellennotiz | uspto-grants-2007_01 |
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