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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580409Generated: October 30, 2026

Potassium Iodide → HCID 67866150, compound

https://huagongshe.com/reaction/580409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMethyl Ethyl KetoneHCID 6569—
Reactant2-Chloro-N,N-dimethylethylamineHCID 7901—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 20135083HCID 20135083—
SolventTolueneHCID 1140—
ProductHCID 67866150HCID 67866150—

Reaction Steps

To 1,3,4,5-tetrahydro-4-(methoxyphenyl)-3-(2-propenyl)-6-(trifluoromethyl)-2H-1-benzazepin-2-one (3.40 g; 9.05 mmole), potassium bicarbonate (1.81 g; 18.1 mmole), and potassium iodide (catalytic amount) suspended in methylethyl ketone (55 ml) was added a 2.15M solution of 2-dimethylaminoethyl chloride (5.1 ml; 10.9 mmole) in toluene, with stirring. After refluxing for ~30 minutes, an additional 5.1 ml of the amine was added, and an additional 1.81 g of potassium bicarbonate was added after 1.5 hours of reflux. After six hours of reflux, the mixture was rotary evaporated and the residue was dissolved into ethyl acetate, and washed with water. The organic layer was dried (magnesium sulfate) and concentrated leaving 4.07 g of viscous, oily free amine of the title compound. This material was flash chromatographed (silica gel/0.5-3% gradient methanol:dichloromethane) and the cis containing fractions were combined and concentrated, dissolved in ether, washed with 1N sodium bicarbonate, dried (magnesium sulfate), and acidified with hydrogen chloride saturated ether. The mixture was concentrated and the white solid triturated in ether. The solid product was collected by suction-filtration, yielding 1.39 g of the title compound; melting point 226°-228° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04752645
Source datasetuspto-grants-1988_06
ORD IDord-e5a2da8f80924e75977fff8a5084e108
Source noteuspto-grants-1988_06