HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 611176Erstellt: 26. Oktober 2026
Acetic Acid → 1-(2-ethylmethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-one
https://huagongshe.com/reaction/611176
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | N-Methylethylamine | HCID 12219 | — |
| Edukt | 1-(5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-one | HCID 19600145 | — |
| Produkt | 1-(2-ethylmethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-one | HCID 67584926 | — |
Reaktionsschritte
To a solution of 0.400 g (1.345 mmol) of 1-(5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-one in 20 ml of acetic acid, 0.14 ml (1.6 mmol) of N-Ethylmethylamine and 0.13 9 (1.6 mmol) of 37% aqueous formaldehyde were added, followed by stirring at 100° C. for 1 hour. After the solvent was distilled off under reduced pressure, the residual solution was alkalified with aqueous sodium hydroxide and extracted with dichloromethane 3 times. The combined organic layer was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (ethyl acetate to ethyl acetate/methanol=4/1) to yield the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05998433 |
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| Quelldatensatz | uspto-grants-1999_12 |
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| ORD ID | ord-6b244c45fd7d4ddeab8e414b0545dfed |
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| Quellennotiz | uspto-grants-1999_12 |
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