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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktQuinuclidine, 3-amino-, dihydrochlorideHCID 197853—
Edukt2-Propoxybenzoyl chlorideHCID 15921913—
EduktBarium hydroxide, octahydrateHCID 17749109—
LösungsmittelCarbon DioxideHCID 280—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(1-Azabicyclo[2.2.2]oct-3-yl)-2-propoxybenzamide hydrochlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04722834
Quelldatensatzuspto-grants-1988_02
ORD IDord-03d1b8f05e4141739d0b6c4cac54a2f6
Quellennotizuspto-grants-1988_02