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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821425Generated: November 3, 2026

Sodium Iodide → 5-Methoxy-4-[3-(morpholin-4-yl)propyloxy]-2-nitrobenzaldehyde

https://huagongshe.com/reaction/1821425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMorpholineHCID 8083—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(3-Chloropropyloxy)-5-methoxy-2-nitrobenzaldehydeHCID 86628219—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5-Methoxy-4-[3-(morpholin-4-yl)propyloxy]-2-nitrobenzaldehydeHCID 8662821854%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-(3-Chloropropyloxy)-5-methoxy-2-nitrobenzaldehyde (0.40 g, 1.5 mmol) was dissolved in toluene (6.0 mL) and the solution was added with potassium carbonate (1.0 g, 7.3 mmol) dissolved in morpholine (0.38 mL, 4.4 mmol), sodium iodide (0.44 g, 2.9 mmol), tetrabutylammonium bromide (24 mg, 0.007 mmol) and water (2.0 mL), followed by stirring at 100° C. for 19 hours. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The filtrate was purified by silica gel column chromatography (hexane/ethyl acetate=100/0 to 0/100) and concentrated to obtain 5-methoxy-4-[3-(morpholin-4-yl)propyloxy]-2-nitrobenzaldehyde (0.26 g, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605272B2
Source datasetuspto-grants-2009_10
ORD IDord-85a5bf4bc6f04f29b8200ec1b4f667b3
Source noteuspto-grants-2009_10