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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386298Generated: October 25, 2026

Potassium Iodide → 3-Methoxy-4-[3-(1-pyrrolidinyl)propoxy]-benzoic acid Hydrochloride

https://huagongshe.com/reaction/1386298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantVanillic AcidHCID 8468—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(3-Chloropropyl)-pyrrolidineHCID 11321028—
SolventDimethylformamideHCID 6228—
Product3-Methoxy-4-[3-(1-pyrrolidinyl)propoxy]-benzoic acid HydrochlorideHCID 2482023677.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-hydroxy-3-methoxybenzoic acid (8.4 g, 50 mmol), 3-(pyrrolidin-1-yl)propyl chloride (14.75 g, 0.1 mol), (prepared according to J. Am. Chem. Soc. 1955, 77. 2272), potassium carbonate (13.8 g, 0.1 mol) and potassium iodide (1.66 g, 10 mmol) in DMF (150 ml) was stirred and heated at 100° C. for 3 hours. The mixture was allowed to cool and the insolubles were removed by filtration and the volatiles were removed from the filtrate by evaporation. The residue was dissolved in ethanol (75ml), 2M aqueous sodium hydroxide (75 ml) was added and the mixture was heated at 90° C. for 2 hours. The mixture was concentrated by evaporation, 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 dilute hydrochloric acid (pH2.2). The methanol was removed by evaporation and the aqueous residue was freeze dried to give 3-methoxy-4-(3-(pyrrolidin-1-yl)propoxy)benzoic acid hydrochloride (12.2 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265411B1
Source datasetuspto-grants-2001_07
ORD IDord-14daca9212164ccbad684da1e563796c
Source noteuspto-grants-2001_07