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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44824생성일: 2026년 10월 23일

Iodobenzene → 4-Bromo-3-phenylpyridine

https://huagongshe.com/ko/reaction/44824

반응식

참여 물질

역할이름HCID투입량
반응물IodobenzeneHCID 11575—
반응물4-Bromopyridinium chlorideHCID 88100—
반응물Lithium diisopropylamideHCID 2724682—
촉매ZincchlorideHCID 3007855—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
용매Ammonium ChlorideHCID 25517—
생성물4-Bromo-3-phenylpyridineHCID 2762939153.7%

반응 조건

온도-78 °C

반응 단계

4-bromopyridine hydrochloride (1-BA-2, 1 g, 5.14 mmol) was dissolved in 5.1 mL of THF and the resulting solution was cooled to −78° C. LDA (10.28 mL of a 1 M solution in THF) was added over 10 minutes and the reaction mixture became brown. After stirring for 30 minutes, ZnCl2 (10.3 mL of a 0.5 M solution in THF) was added over 10 minutes and the resulting mixture was stirred for 10 minutes and then allowed to warm to rt. Iodobenzene (0.229 mL, 2.06 mmol) and Pd(PPh3)4 (593 mg, 0.514 mmol) were added and the resulting mixture was stirred under reflux for 2 h. The reaction mixture was diluted with aqueous saturated ammonium chloride and extracted with ethyl acetate. The organic phase was dried over Na2SO4 and evaporated. The residue was purified by silica column (hexane:EtOAc) to give 4-bromo-3-phenylpyridine (2-BA-2, 741 mg, 62%); LCMS: 234.0 m/z (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541418B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-d42ba659b44e41ba80009cd5ab48e771
출처 메모uspto-grants-2013_09