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HRID 1910562作成日:2026年10月27日

2,4-Difluoronitrobenzene → N-(1-(3-bromophenyl)ethyl)-5-fluoro-2-nitrobenzenamine

https://huagongshe.com/reaction/1910562

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-DifluoronitrobenzeneHCID 67967—
反応物DiisopropylethylamineHCID 81531—
反応物1-(3-Bromophenyl)ethanamineHCID 16785764—
溶媒AcetonitrileHCID 6342—
生成物N-(1-(3-bromophenyl)ethyl)-5-fluoro-2-nitrobenzenamineHCID 5870727174%

反応手順

A mixture of 1-(3-bromophenyl)ethanamine (1.0 g, 5.0 mmol), 2,4-difluoro-1-nitrobenzene (0.8 g, 5.0 mmol), N,N-diisopropylethylamine (1.7 mL, 10.0 mmol) and acetonitrile (20 mL) was stirred for 18 h and concentrated in vacuo. The residue was dissolved in ethyl acetate; this solution was washed with water, dried over Na2SO4 and concentrated in vacuo to yield the title compounds as a yellow oil (1.25 g, 74%). 1H NMR (400 MHz, CDCl3): δ 8.51 (d, 1 H), 8.25 (m, 1 H), 7.48 (s, 1 H), 7.41 (m, 1 H), 7.25 (m, 2 H), 6.36 (m, 1 H), 6.24 (m, 1 H), 4.55 (m, 1 H), 1.63 (d, 3 H). MS (ESI) m/z: Calculated: 338; Observed: 339 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08604021B2
出典データセットuspto-grants-2013_12
ORD IDord-e1b40f61bab34f9eb067846044c44b58
出典メモuspto-grants-2013_12