HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3762Erstellt: 24. Oktober 2026
Quinuclidine, 3-amino-, dihydrochloride → N-(1-Azabicyclo[2.2.2]oct-3-yl)-2-propoxybenzamide hydrochloride
https://huagongshe.com/de/reaction/3762
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Quinuclidine, 3-amino-, dihydrochloride | HCID 197853 | — |
| Edukt | 2-Propoxybenzoyl chloride | HCID 15921913 | — |
| Edukt | Barium hydroxide, octahydrate | HCID 17749109 | — |
| Lösungsmittel | Carbon Dioxide | HCID 280 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-(1-Azabicyclo[2.2.2]oct-3-yl)-2-propoxybenzamide hydrochloride | HCID 13630995 | — |
Reaktionsschritte
To a solution of 3.82 g (0.0192 mole) of 3-amino quinuclidine dihydrochloride in about 25 ml of carbon dioxide-free water was added 8 g (0.025 mole) of barium hydroxide octahydrate. The mixture was warmed for 5 minutes and then dried to a powder on a rotary evaporator. While protecting from contamination with carbon dioxide in the atmosphere, the powder was extracted in sequence with hot benzene and a 1:1 mixture of benzene-methylene chloride solution. The combined extracts were dried over magnesium sulfate and the mixture filtered. To the filtrate with agitation was added dropwise a solution of 3.4 g (0.0171 mole) of 2-propoxybenzoyl chloride in 50 ml of methylene chloride. The mixture was warmed on a steam bath to evaporate about 75% of the methylene chloride. Ligroin (60-110) was added and the mixture solidified. The solid was recrystallized from anhydrous ethyl alcohol to give 3.9 g (62.0%), m.p. 210°-211° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04722834 |
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| Quelldatensatz | uspto-grants-1988_02 |
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| ORD ID | ord-03d1b8f05e4141739d0b6c4cac54a2f6 |
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| Quellennotiz | uspto-grants-1988_02 |
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