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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481782Generated: October 30, 2026

Potassium Iodide → 2-[2-(Ethoxycarbonyl)ethyl]-1-methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/481782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantEthyl 2-bromopropionateHCID 79040—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Methyl-7-nitro-1,2,3,4-tetrahydroisoquinolineHCID 21584311—
SolventEthanolHCID 702—
Product2-[2-(Ethoxycarbonyl)ethyl]-1-methyl-7-nitro-1,2,3,4-tetrahydroisoquinolineHCID 1906717465.8%

Reaction Steps

0.90 g of 1-methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline was dissolved in 20 ml of ethanol, and 1.97 g of sodium bicarbonate, 2.55 g of ethyl bromopropionate, and a catalytic amount of potassium iodide were added to the solution. The solution was heated overnight under ref lux with stirring, and extracted with ethyl acetate. After washing with water and saturated aqueous solution of sodium chloride, the solution was dried with anhydrous sodium sulfate. The desiccant was separated by filtration, and the filtrate was purified by silica gel column chromatography to obtain 0.90 g of 2-[2-(ethoxycarbonyl)ethyl]-1-methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline, which was an oily product (yield: 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789595
Source datasetuspto-grants-1998_08
ORD IDord-8a206188ea6741718409527477fd8814
Source noteuspto-grants-1998_08