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HRID 2278279作成日:2026年10月25日

Potassium Carbonate → HCID 89677182、化合物

https://huagongshe.com/reaction/2278279

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1,4-DioxaneHCID 31275—
反応物3-Tolylboronic acidHCID 2733950—
反応物tert-Butyl 4-(4-bromo-2-phenoxybenzyl)piperazine-1-carboxylateHCID 89677060—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
生成物HCID 89677182HCID 8967718281.4%

反応条件

温度80 °C

反応手順

A 100 mL round-bottom flask was purged with and maintained an inert atmosphere of nitrogen then charged with tert-butyl 4-[(4-bromo-2-phenoxyphenyl)methyl]piperazine-1-carboxylate (1.20 g, 2.68 mmol, 1.00 equiv), (3-methylphenyl)boronic acid (0.730 g, 5.37 mmol, 2.00 equiv), Pd(PPh3)4 (0.310 g, 0.270 mmol, 0.10 equiv), potassium carbonate (1.10 g, 7.96 mmol, 2.97 equiv), dioxane (12 mL), and water (2 mL). The resulting solution was stirred overnight at 80° C. and then diluted with water (10 mL) and extracted with ethyl acetate (3×10 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was chromatographed on a silica gel column with ethyl acetate/petroleum ether (1/9) to provide 1.00 g (81% yield) of tert-butyl 4-[[4-(3-methylphenyl)-2-phenoxyphenyl]methyl]piperazine-1-carboxylate as yellow oil. LCMS (ESI, m/z): 459 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09133148B2
出典データセットuspto-grants-2015_09
ORD IDord-8179d82a05e14686b4282b4e710bd788
出典メモuspto-grants-2015_09