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HRID 454005Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/454005

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktVanillic AcidHCID 8468—
EduktPotassium CarbonateHCID 11430—
Edukt1-(3-Chloropropyl)-pyrrolidineHCID 11321028—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-Methoxy-4-[3-(1-pyrrolidinyl)propoxy]-benzoic acid HydrochlorideHCID 2482023677,3%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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), (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 (75 ml), 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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08492560B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-62999f3dce0d4398a39d059cd2a0c7f4
Quellennotizuspto-grants-2013_07