HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413466Generated: October 26, 2026
Quinuclidine, 3-amino-, dihydrochloride → N-(1-Azabicyclo[2.2.2]oct-3-yl)-2-propoxybenzamide hydrochloride
https://huagongshe.com/reaction/2413466
Participants
| Role | Name | HCID | Charge |
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| Reactant | Quinuclidine, 3-amino-, dihydrochloride | HCID 197853 | — |
| Reactant | 2-Propoxybenzoyl chloride | HCID 15921913 | — |
| Reactant | Barium hydroxide, octahydrate | HCID 17749109 | — |
| Solvent | Carbon Dioxide | HCID 280 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1-Azabicyclo[2.2.2]oct-3-yl)-2-propoxybenzamide hydrochloride | HCID 13630995 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04717563 |
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| Source dataset | uspto-grants-1988_01 |
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| ORD ID | ord-006b05c9d760401e9f2b1a4a08bf3428 |
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| Source note | uspto-grants-1988_01 |
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