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HRID 454005作成日:2026年10月26日

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

https://huagongshe.com/reaction/454005

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Vanillic AcidHCID 8468—
反応物Potassium CarbonateHCID 11430—
反応物1-(3-Chloropropyl)-pyrrolidineHCID 11321028—
溶媒DimethylformamideHCID 6228—
生成物3-Methoxy-4-[3-(1-pyrrolidinyl)propoxy]-benzoic acid HydrochlorideHCID 2482023677.3%

反応条件

温度100 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08492560B2
出典データセットuspto-grants-2013_07
ORD IDord-62999f3dce0d4398a39d059cd2a0c7f4
出典メモuspto-grants-2013_07