HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1007899Erstellt: 24. Oktober 2026
Hydrochloric Acid → N-[3-(2-benzo[b]thiophen-5-ylethoxy)propyl]-N,N-diethylamine
https://huagongshe.com/de/reaction/1007899
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Diethylamine | HCID 8021 | — |
| Edukt | 5-[2-(3-Chloropropyloxy)ethyl]benzo[b]thiophene | HCID 21990069 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | N-[3-(2-benzo[b]thiophen-5-ylethoxy)propyl]-N,N-diethylamine | HCID 22666289 | — |
Reaktionsschritte
In 6 mL of N,N-dimethylformamide is dissolved 0.80 g of 5-[2-(3-chloropropyloxy)ethyl]benzo[b]-thiophene, to which is added 3.2 mL of diethylamine. The mixture is stirred in an ampoule at 100° C. for 10 hours. After cooling, the reaction mixture is introduced into a mixture of water and ethyl acetate, pH is adjusted to 1.0 with 6 mol/L hydrochloric acid, and the aqueous layer is separated. Ethyl acetate is added to the aqueous layer, pH is adjusted to 10.0 with 5 mol/L aqueous solution of sodium hydroxide, and the organic layer is separated. The organic layer is washed with water and saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, the solvent is distilled off under reduced pressure, and the residue is purified by column chromatography (eluent: chloroform:methanol=10:1 to 4:1). Thus, 0.48 g of N-[3-(2-benzo[b]thiophen-5-ylethoxy)propyl]-N,N-diethylamine is obtained as an oily product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06797726B1 |
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| Quelldatensatz | uspto-grants-2004_09 |
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| ORD ID | ord-4a8da577d4194a3789bebcea626b4cf3 |
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| Quellennotiz | uspto-grants-2004_09 |
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