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HRID 1791538생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1791538

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참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Vanillic AcidHCID 8468—
반응물Potassium CarbonateHCID 11430—
반응물1-(3-Chloropropyl)-pyrrolidineHCID 11321028—
용매DimethylformamideHCID 6228—
생성물3-Methoxy-4-[3-(1-pyrrolidinyl)propoxy]-benzoic acid HydrochlorideHCID 2482023677.3%

반응 조건

온도100 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07074800B1
출처 데이터셋uspto-grants-2006_07
ORD IDord-e3d1096b942a4a54904d797e6ac7b158
출처 메모uspto-grants-2006_07