HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248848Erstellt: 26. Oktober 2026
Hydrochloric Acid → N-[2-(2,2-dimethylethoxy)ethyl]-N-benzyl-N-methylamine
https://huagongshe.com/reaction/248848
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Isobutanol | HCID 6560 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | N-benzyl-2-chloro-N-methylethanamine | HCID 31968 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | N-[2-(2,2-dimethylethoxy)ethyl]-N-benzyl-N-methylamine | HCID 19762361 | 71,7% |
Reaktionsschritte
A solution of 5.0 g of isobutanol in 50 ml of toluene was added at a temperature of 0° C. to a solution of 3.25 g of sodium hydride in 100 ml of toluene, and the reaction mixture was heated under reflux for 3 hours. 12.4 g of N-benzyl-N-methyl-2-chloroethylamine were then added to the reaction mixture, and the solution was heated under reflux for a further 8 hours. The reaction solution was worked up by cautiously adding 5 ml of methanol and then 100 ml of water, and the pH was then adjusted to pH 2 by adding dilute aqueous hydrochloric acid solution. After shaking, the organic phase was separated and discarded. The aqueous phase was adjusted to pH 13 by addition of aqueous sodium hydroxide solution and extracted with ethyl acetate. The ethyl acetate extract was dried over sodium sulfate, filtered and concentrated. The remaining residue was purified by chromatography on silica gel using n-hexane/ethyl acetate as the eluent. 10.7 g of N-[2-(2,2-dimethylethoxy)ethyl]-N-benzyl-N-methylamine were obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05212173 |
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| Quelldatensatz | uspto-grants-1993_05 |
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| ORD ID | ord-4793b644d643462585a2d79cbdff4e2f |
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| Quellennotiz | uspto-grants-1993_05 |
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