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HRID 1811532作成日:2026年10月27日

Nitrogen → 2-Fluoro-3-trifluoromethyl-4-vinylaniline

https://huagongshe.com/reaction/1811532

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物4-Bromo-2-fluoro-3-(trifluoromethyl)anilineHCID 53669714—
反応物Tributylvinyltin chlorideHCID 86633508—
溶媒DimethylformamideHCID 6228—
生成物2-Fluoro-3-trifluoromethyl-4-vinylanilineHCID 68821544—

反応条件

温度120 °C

反応手順

4-Bromo-2-fluoro-3-trifluoromethylaniline described above (5.0 g, 19.4 mmol) and tributylvinyltin chloride (7.1 g, 20.4 mmol) are added to anhydrous DMF (100 mL). The solution is degassed with N2, palladium tetrakistriphenylphosphine (1.5 g, 1.3 mmol) is added, and the reaction is heated at 120° C. for 18 hours. After cooling, the reaction mixture is partitioned between Et2O and saturated aqueous NaCl. The separated ether layer is washed with fresh saturated aqueous NaCl (2×), dried with Na2SO4, and concentrated under reduced pressure. The residue is purified by flash chromatography eluting with 5, then 10, then 20% EtOAc in hexanes to give the desired product, 2-fluoro-3-trifluoromethyl-4-vinylaniline.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08362294B2
出典データセットuspto-grants-2013_01
ORD IDord-b23fb36a00544ed0bba69c20bf831d51
出典メモuspto-grants-2013_01