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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032663Generated: October 26, 2026

Sodium Iodide → N-Methyl-2-(4-nitrophenoxy)-N-[2-(4-nitrophenyl)ethyl]ethanamine

https://huagongshe.com/reaction/1032663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-Chloroethoxy)-4-nitrobenzeneHCID 2764587—
ReactantN-methyl-4-nitrophenethylamineHCID 2794239—
SolventAcetonitrileHCID 6342—
ProductN-Methyl-2-(4-nitrophenoxy)-N-[2-(4-nitrophenyl)ethyl]ethanamineHCID 1464509071.6%

Reaction Steps

To a solution of N-methyl-4-nitrophenethylamine (1.5 g) (J.O.C., [1956], 21, 45) and 2-[4-nitrophenoxy]ethyl chloride (1.55 g) (C.A., [1955], 49, 3163e) in acetonitrile (50 ml) was added potassium carbonate (1.25 g) and sodium iodide (1.2 g) and the suspension was stirred at reflux for 72 hours. After evaporation to dryness, the residual oily solid was partitioned between a 2N aqueous sodium bicarbonate solution and ethyl acetate. After two further extractions with ethyl acetate, the organic portions were combined, washed with a saturated aqueous brine solution, dried over magnesium sulphate, filtered and evaporated. The resultant orange solid (2.7 g) was crystallised from ethanol to give the title compound, (1.9 g), m.p. 74°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04959366
Source datasetuspto-grants-1990_09
ORD IDord-7a7833b0155442a1b969b23ea2d0a381
Source noteuspto-grants-1990_09