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HRID 228073作成日:2026年10月25日

Potassium Carbonate → Methyl 2-[4-benzylpiperazinyl]benzoate

https://huagongshe.com/reaction/228073

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Benzoic acid, 2-fluoro-, methyl esterHCID 67854—
反応物1-BenzylpiperazineHCID 75994—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 2-[4-benzylpiperazinyl]benzoateHCID 2193510158%

反応条件

温度150 °C

反応手順

To a 250 mL pressure bottle equipped with magnetic stirring was added methyl 2-fluorobenzoate (Lancaster Synthesis Inc.) (3.0 g, 20 mmol), 1-benzylpiperazine (Aldrich) (3.8 g, 22 mmol) and K2CO3 (3.0 g, 22 mmol) in DMF (100 mL). The mixture was heated at 150° C. for 12 h. After cooling to RT the reaction was diluted with EtOAc (100 mL) and H2O was added. The organic layer was separated and washed with H2O, brine, dried over Na2SO4, filtered and concentrated in vacuo to afford a brown oil. The crude material was purified by column chromatography (4:1 hexanes-EtOAc) to give the title compound as a white foam (3.6 g). MS (ESI, pos. ion) m/z: 311 (M+H). Calc'd for C19H22N2O2: 310.17.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560460B2
出典データセットuspto-grants-2009_07
ORD IDord-e8696c8d17eb438c9f752089da2f8e11
出典メモuspto-grants-2009_07