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HRID 19792作成日:2026年10月24日

Iodine → 2-Cyclopropyl-1-fluoro-4-iodobenzene

https://huagongshe.com/ja/reaction/19792

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Isoamyl NitriteHCID 8053—
反応物Cesium iodideHCID 24601—
反応物3-Cyclopropyl-4-fluoroanilineHCID 57416303—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2-Cyclopropyl-1-fluoro-4-iodobenzeneHCID 6856411072%

反応条件

温度60 °C

反応手順

To a solution of 3-cyclopropyl-4-fluorophenylamine (210 mg, 1.39 mmol) in DME (1.5 ml) was added caesium iodide (360 mg, 1.39 mmol), cuprous iodide (82 mg, 0.43 mmol), iodine (176 mg, 0.70 mmol) and isoamyl nitrite (1.11 ml, 8.34 mmol). The reaction mixture was heated to 60° C. for 2 h. The reaction mixture was cooled to RT and partitioned between pentane and sat. NH4Cl solution. The organic layer was separated, washed with 5% sodium thiosulfite and brine, dried (MgSO4), filtered and concentrated in vacuo to give a residue which was purified by flash column chromatography (100% pentane) to yield the desired 2-cyclopropyl-1-fluoro-4-iodobenzene (262 mg, 72%) as a colorless oil. 1H NMR (CDCl3, 300 MHz): 7.40 (m, 1H), 7.17 (m, 1H), 6.76 (m, 1H), 2.02 (m, 1H), 1.03-0.96 (m, 2H), 0.74-0.68 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745477B2
出典データセットuspto-grants-2010_06
ORD IDord-27835b63b9e04a92b1eee076253f85c2
出典メモuspto-grants-2010_06