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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386253Generated: October 30, 2026

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

https://huagongshe.com/reaction/1386253

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 filtrate evaporated. The residue was dissolved in ethanol (50 ml), 2M sodium hydroxide (50 ml) was added and the mixture 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 numberUS06265411B1
Source datasetuspto-grants-2001_07
ORD IDord-12ee9487f4bb491c8c0c121595a05c03
Source noteuspto-grants-2001_07