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HRID 336256作成日:2026年10月26日

Lithium Hydroxide → 3-Cyano-4-(2-methylpiperidin-1-yl)benzoic acid

https://huagongshe.com/reaction/336256

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium HydroxideHCID 3939—
反応物2-MethylpiperidineHCID 7974—
反応物Methyl 3-cyano-4-fluorobenzoateHCID 45790123—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-Cyano-4-(2-methylpiperidin-1-yl)benzoic acidHCID 5949570180.2%

反応手順

2-Methylpiperidine (744 mg; 7.5 mmol; 5 eq.) was added to a solution of methyl 3-cyano-4-fluorobenzoate (269 mg; 1.5 mmol; 1 eq.) in DMF (2 mL) and the resulting mixture was stirred at room temperature for 2 days. The solution was partitioned between ethyl acetate and water and the phases separated. The organic layer was washed with HCl 0.1M then brine, dried over magnesium sulfate and concentrated in vacuo. The residue was taken up in THF (5 mL) and LiOH (126 mg; 3 mmol; 2 eq.) then water (5 mL) were added and the reaction mixture was stirred at room temperature for 5 hours. The resulting solution was diluted with water and washed with Et2O. The aqueous layer was acidified to pH 2 with HCl 0.1M and extracted with ethyl acetate. The organic phase was dried over magnesium sulfate and concentrated in vacuo to afford the title compound (294 mg, 80%) as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889668B2
出典データセットuspto-grants-2014_11
ORD IDord-6bc00f824d174c799cec5f645b14d410
出典メモuspto-grants-2014_11