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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596823Generated: October 31, 2026

Hydrochloric Acid → HCID 21448657, compound

https://huagongshe.com/reaction/596823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 19088473HCID 19088473—
Reactant2-Azabicyclo[2.2.2]octane hydrochlorideHCID 21984844—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventIsopropanolHCID 3776—
ProductHCID 21448657HCID 21448657—

Reaction Steps

A mixture of 6.5 parts 5-cyano-5-(2-bromoethyl)10,11-dihydro-5H-dibenzo[a,d]cycloheptene, 4.0 parts 2-azabicyclo[2.2.2]octane hydrochloride and 4.0 parts potassium carbonate in 88 parts N,N-dimethylsulfoxide and 20 parts water is heated at reflux for about 4 hours. After cooling, the reaction mixture is diluted with water, resulting in the formation of an oil. The water layer is decanted and the oil dissolved in ethyl ether. The ethereal solution is washed twice with water, once with a saturated sodium chloride solution, dried over anhydrous sodium sulfate and filtered. The solvent is removed to give an oil which is treated with a solution of hydrogen chloride in isopropanol. Addition of ethyl ether results in a precipitate that is separated, washed with ether and dried to afford-5-cyano-5[2-(2-azabicyclo[2.2.2]oct-2-yl)ethyl]-10,11-dihydro-5H-dibenzo[a,d]cycloheptene hydrochloride. This compound is represented by the following structural formula. ##STR14##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04012393
Source datasetuspto-grants-1977_03
ORD IDord-3fb9f6d6320d4adfbe98081382fc8a98
Source noteuspto-grants-1977_03