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HRID 44824作成日:2026年10月25日

Iodobenzene → 4-Bromo-3-phenylpyridine

https://huagongshe.com/reaction/44824

反応式

関与物質

役割名称HCID仕込み量
反応物IodobenzeneHCID 11575—
反応物4-Bromopyridinium chlorideHCID 88100—
反応物Lithium diisopropylamideHCID 2724682—
触媒ZincchlorideHCID 3007855—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
溶媒Ammonium ChlorideHCID 25517—
生成物4-Bromo-3-phenylpyridineHCID 2762939153.7%

反応条件

温度-78 °C

反応手順

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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541418B2
出典データセットuspto-grants-2013_09
ORD IDord-d42ba659b44e41ba80009cd5ab48e771
出典メモuspto-grants-2013_09