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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596824Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 21448660, compound

https://huagongshe.com/reaction/596824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium CarbonateHCID 11430—
Reactant12-Cyano-12-(2-bromoethyl)-5,6,7,12-tetrahydrodibenzo[a,d]cycloocteneHCID 21448662—
Reactant2-Azabicyclo[2.2.2]octane hydrochlorideHCID 21984844—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductHCID 21448660HCID 21448660—

Reaction Conditions

Temperature100 °C

Reaction Steps

3.1 Parts 12-cyano-12-(2-bromoethyl)-5,6,7,12-tetrahydrodibenzo[a,d]cyclooctene, 1.8 parts 2-azabicyclo[2.2.2]octane hydrochloride, 1.8 parts potassium carbonate, 44 parts dimethylsulfoxide and 10 parts water are combined, heated at 100° C. for about 4 hours, and then poured into an ice-water mixture. The resulting gummy precipitate is dissolved in a mixture of ethyl ether and methylene chloride. The organic phase is separated, washed three times with water, dried with sodium sulfate, filtered, and the solvents removed to leave an oil. This oil is dissolved with a solution of HC1 in isopropanol, and precipitated with ethyl ether to give 12-cyano12-[2-(2-azabicyclo[2.2.2]oct-2-yl)ethyl]-5,6,7,12-tetrahydrodibenzo[a,d]cyclooctene hydrochloride. This compound is represented by the following structural formula. ##STR17##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04012393
Source datasetuspto-grants-1977_03
ORD IDord-daee9cc1d34847c199d396dac081de17
Source noteuspto-grants-1977_03