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HRID 50565Erstellt: 24. Oktober 2026
Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → (E)-3-[4-(2-Pyridinyl)phenyl]-2-propenal
https://huagongshe.com/de/reaction/50565
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- | HCID 112414 | — |
| Edukt | 4-Pyridin-2-ylbenzaldehyde | HCID 1515240 | — |
| Edukt | (1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide | HCID 2724194 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Potassium Carbonate | HCID 11430 | — |
| Produkt | (E)-3-[4-(2-Pyridinyl)phenyl]-2-propenal | HCID 22630962 | 89% |
Reaktionsschritte
A mixture of 4-(2-pyridinyl)-benzaldehyde (1.76 g, 9.58 mmol), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (6.45 g, 15.02 mmol), and TDA-1 (Tris(3,6-dioxaheptyl)amine, 3.20 mL, 10.00 mmol) in dichloromethane (50 mL) and sat. aq. K2CO3 (50 mL) was heated to reflux for 20 h. The layers were separated and the aqueous layer was extracted with dichloromethane (2×25 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (MgSO4), and concentrated. THF (25 mL) and 10% HCl (25 mL) were added and the mixture was stirred for 1 h at rt. The reaction mixture was cooled to 0° C., made basic with 10% NaOH, and extracted with ethyl acetate (3×25 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (MgSO4), and concentrated. Purification by chromatography (SiO2, 3:1 hexane/ethyl acetate) provided 1.69 g (89%) of the title compound as a yellow solid. MS 210 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06713455B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-bad2f943fd7c49719d72604fed49f6af |
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| Quellennotiz | uspto-grants-2004_03 |
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