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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597209Generated: November 2, 2026

Potassium Iodide → 3-Methoxy-4-(3-morpholinopropoxy)benzoic acid

https://huagongshe.com/reaction/1597209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantVanillic AcidHCID 8468—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(3-Chloropropyl)morpholineHCID 95834—
SolventDimethylformamideHCID 6228—
Product3-Methoxy-4-(3-morpholinopropoxy)benzoic acidHCID 21699284109.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-hydroxy-3-methoxybenzoic acid (4.5 g, 26.8 mmol), 3-morpholinopropyl chloride (9.5 g, 58.0 mmol), (prepared according to J. Am. Chem. Soc. 1945, 67, 736), potassium carbonate (8.0 g, 58 mmol), potassium iodide (1.0 g, 0.22 mmol) and DMF (80 ml) was stirred and heated at 100° C. for 3 hours. The solid was removed by filtration and the volatiles were removed from the filtrate by evaporation. The residue was dissolved in ethanol (50 ml), 2M sodium hydroxide (50 ml) was added and the mixture was heated at 90° C. for 2 hours. After partial evaporation, the mixture was acidified with concentrated hydrochloric acid, washed with ether and then subjected to purification on a Diaion (trade mark of Mitsubishi) HP20SS resin column, eluting with water and then with a gradient of methanol (0 to 25%) in hydrochloric acid (pH2). Partial evaporation of the solvents and lyophilisation gave 3-methoxy-4-(3-morpholinopropoxy)benzoic acid (8.65 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294532B1
Source datasetuspto-grants-2001_09
ORD IDord-032e2f981db2462197ebc1997c469494
Source noteuspto-grants-2001_09