Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3761Generated: October 25, 2026

Water → N-(1-Azabicyclo[2.2.2]oct-3-yl)-2,4-dimethoxybenzamide hydrochloride

https://huagongshe.com/reaction/3761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantQuinuclidine, 3-amino-, dihydrochlorideHCID 197853—
Reactant2,4-Dimethoxybenzoyl chlorideHCID 2734719—
SolventChloroformHCID 6212—
ProductN-(1-Azabicyclo[2.2.2]oct-3-yl)-2,4-dimethoxybenzamide hydrochlorideHCID 1327233023.7%

Reaction Steps

A mixture of 3-aminoquinuclidine dihydrochloride, 6.95 g, (0.349), 2,4-dimethoxybenzoyl chloride, 700 g, (0.0349 mole), anhydrous sodium carbonate, 36.99 g, (0.349 mole), 175 ml water, and 175 ml chloroform was stirred rapidly to achieve good mixing of the 2 layers for 20 hrs. The chloroform layer was then separated, washed with water, dried over anhydrous magnesium sulfate, and concentrated to an impure oil. The oil was triturated twice with 20 ml portions of petroleum ether to remove some impurities. The oil was then dissolved in diethyl ether and filtered to remove a small amount of insoluble material. The filtrate was treated with ethereal hydrogen chloride and the resulting salt collected to yield 2.70 g (23.7% yield) white solid. The salt was recrystallized from ethanol-isopropyl ether. Further recrystallization from methanol-ethyl ether yielded a white solid, m.p. 211°-212° C. The NMR analysis was satisfactory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04722834
Source datasetuspto-grants-1988_02
ORD IDord-217b10af343044bfa5761f4da10eaeb8
Source noteuspto-grants-1988_02