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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454005생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/454005

반응식

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 번호US08492560B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-62999f3dce0d4398a39d059cd2a0c7f4
출처 메모uspto-grants-2013_07