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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/520

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DibromobenzeneHCID 7804—
반응물Methyl Pyrrolidine-3-carboxylateHCID 4114360—
시약Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물Methyl 1-(4-bromophenyl)pyrrolidine-3-carboxylateHCID 8398169331.6%

반응 조건

온도85 °C

반응 단계

A suspension of methyl pyrrolidine-3-carboxylate (2.1 g, 16.26 mmol), 1,4-dibromobenzene (3.84 g, 16.26 mmol), TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.372 g, 0.41 mmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.759 g, 1.22 mmol) and Sodium Tert-Butoxide (1.875 g, 19.51 mmol) in anhydrous toluene (60 mL) was stirred at 85 °C under nitrogen for 16 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 5 to 20% EtOAc in heptane. Pure fractions were evaporated to dryness to afford methyl 1-(4-bromophenyl)pyrrolidine-3-carboxylate (1.460 g, 31.6 %) as a yellow solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-7673f35cb6ca4307811eaa7801ce679c
출처 메모750 AstraZeneca ELN dataset