HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 963652Erstellt: 24. Oktober 2026
Toluene → 2-[5-(Benzyloxy)-2-nitroanilino]propionaldehyde dimethyl acetal
https://huagongshe.com/de/reaction/963652
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2,2-Dimethoxy-1-methylethylamine | HCID 93658 | — |
| Edukt | 4-(Benzyloxy)-2-chloro-1-nitrobenzene | HCID 819861 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | 2-[5-(Benzyloxy)-2-nitroanilino]propionaldehyde dimethyl acetal | HCID 19083116 | — |
Reaktionsschritte
A mixture of benzyl 3-chloro-4-nitrophenyl ether (48.2 g, 0.183 mole), 2-aminopropionaldehyde dimethyl acetal (65.3 g, 0.55 mole), potassium carbonate (101 g, 0.73 mole) and toluene in dry dimethyl sulfoxide, under nitrogen, is stirred at 99°-105° C. for 20 hours, cooled to room temperature and filtered. The filter cake is washed with ether. The combined filtrates are mixed with ice water. The phases are separated and the aqueous phase is extracted with ether. The ether extracts are combined with the organic phase. The combined organic phase is washed with six portions of water, dried (Na2SO4) and concentrated in vacuo to give an oil residue which is crystallized in methanol to afford the title product as a yellow solid, 39.6 g (64.5%). A sample is recrystallized from methanol to afford a yellow solid, mp 57°-62° C., identified by elemental and NMR analyses.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05763615 |
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| Quelldatensatz | uspto-grants-1998_06 |
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| ORD ID | ord-18fc9b6dbc484a6e8834325bb1a74df5 |
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| Quellennotiz | uspto-grants-1998_06 |
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