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HRID 551作成日:2026年10月23日

Piperidine → 3-Chloro-4-(piperidin-1-yl)benzoic acid

https://huagongshe.com/ja/reaction/551

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物4-Bromo-3-chlorobenzoic acidHCID 12594302—
試薬Sodium t-butoxideHCID 23676156—
触媒Binap, (A+-)-HCID 634876—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物3-Chloro-4-(piperidin-1-yl)benzoic acidHCID 1895623110%

反応条件

温度80 °C

反応手順

4-bromo-3-chlorobenzoic acid (0.353 g, 1.5 mmol), piperidine (0.234 mL, 2.25 mmol), and sodium tert-butoxide (0.216 g, 2.25 mmol) were stirred together under N2 and heated to 80 °C. Pd2(dba)3 (0.014 g, 0.015 mmol), and BINAP (0.031 g, 0.05 mmol) were mixed in toluene (2 mL) and then added to the mixture and stirred at 110 °C overnight. LCMS showed a very small amount of desired product (~2%). The reaction mixture was degassed with N2 for 30 minutes, then addtional Pd/ Binap was added. The reaction was again heated to 110 C. LCMS showed a small amount of desired product (~10%) but mostly still starting material. The desired product was not isolated from this reaction.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-398e791076cd44778e3b80090d8d8371
出典メモ750 AstraZeneca ELN dataset