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HRID 519作成日:2026年10月24日

1,4-Dibromobenzene → Methyl 1-(4-bromophenyl)pyrrolidine-3-carboxylate

https://huagongshe.com/ja/reaction/519

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DibromobenzeneHCID 7804—
反応物Methyl Pyrrolidine-3-carboxylateHCID 4114360—
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Methyl 1-(4-bromophenyl)pyrrolidine-3-carboxylateHCID 8398169329.15%

反応条件

温度85 °C

反応手順

A suspension of methyl pyrrolidine-3-carboxylate (800 mg, 6.19 mmol), 1,4-dibromobenzene (1461 mg, 6.19 mmol), TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (142 mg, 0.15 mmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (289 mg, 0.46 mmol) and Sodium Tert-Butoxide (714 mg, 7.43 mmol) in anhydrous toluene (30 mL) was stirred at 85 °C under nitrogen for 4 hours. The reaction was cooled to ambient temperature, diluted with Ether (100 mL) and filtered through celite. The filtrate was evaporated in vacuo to yield crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in heptane. Pure fractions were evaporated to dryness to afford methyl 1-(4-bromophenyl)pyrrolidine-3-carboxylate (513 mg, 29.1 %) as a yellow solid.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-cb0ae83e039e422babb6d81e64a4df69
出典メモ750 AstraZeneca ELN dataset