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HRID 565686Erstellt: 26. Oktober 2026
Triethylamine → 2,3-Dihydro-2,4,6,7-tetramethyl-2-[[4-(2-phenylethyl)-1-piperidinyl]methyl]-5-benzofuranamine
https://huagongshe.com/reaction/565686
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-(2-Phenylethyl)piperidine | HCID 4341895 | — |
| Edukt | 2-Bromomethyl-2,3-dihydro-2,4,6,7-tetramethyl-5-benzofuranamine | HCID 10850590 | — |
| Lösungsmittel | Sodium Bicarbonate | HCID 516892 | — |
| Produkt | 2,3-Dihydro-2,4,6,7-tetramethyl-2-[[4-(2-phenylethyl)-1-piperidinyl]methyl]-5-benzofuranamine | HCID 15485877 | 42,5% |
Reaktionsschritte
In an autoclave, a mixture of 2-bromomethyl-2,3-dihydro-2,4,6,7-tetramethyl-5-benzofuranamine (1.5 g), 4-(2-phenylethyl)piperidine (2.0 g), and triethylamine (5.3 g) was stirred under argon gas at 180° C. for 15 hours. After cooling, the reaction mixture was diluted with saturated aqueous NaHCO3 and extracted with ethyl acetate. The extract was washed with saturated aqueous NaCl and dried over MgSO4 and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1:1) and recrystallized from diisopropyl ether to provide 0.88 g of the title compound. Yield 42%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06172085B2 |
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| Quelldatensatz | uspto-grants-2001_01 |
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| ORD ID | ord-48191aeed5bb4d0e9fa03d8a3961a655 |
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| Quellennotiz | uspto-grants-2001_01 |
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