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HRID 508344作成日:2026年10月26日

2-Bromo-4-nitroanisole → Benzene, 1-methoxy-4-nitro-2-(1,1,2,2,2-pentafluoroethyl)-

https://huagongshe.com/reaction/508344

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-4-nitroanisoleHCID 78870—
反応物Sodium pentafluoropropionateHCID 2733305—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物Benzene, 1-methoxy-4-nitro-2-(1,1,2,2,2-pentafluoroethyl)-HCID 10730800—

反応条件

温度150 °C

反応手順

To a 250 mL round-bottom flask was added 2-bromo-1-methoxy-4-nitrobenzene (3.5 g, 15.08 mmol), copper(I) iodide (5.75 g, 30.2 mmol), and sodium 2,2,3,3,3-pentafluoropropanoate (5.25 g, 28.2 mmol) in DMF (75 ml) and toluene (25 ml) to give a tan suspension. The mixture was heated at 150° C. and toluene was removed by a Dean-Stark trap. The mixture was heated at 155° C. for 6 h under nitrogen, cooled and poured into 100 mL of water and 100 mL of ether, filtered through a 1-inch plug of Celite and the plug was rinsed with ether. The filtrate layers were separated. The organic layer was washed with brine, dried (Na2SO4) filtered and concentrated. The dark oil was flash chromatographed on an Isco 40 g silica cartridge eluting with 4:1 hexane/EtOAc to give a yellow oil that was a (3:1) mix of desired material and starting material (1.5 g, 37%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09095590B2
出典データセットuspto-grants-2015_08
ORD IDord-8643760b00ff4365a20fb7274db56b44
出典メモuspto-grants-2015_08