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HRID 576583作成日:2026年10月26日

2-Fluoro-4-nitroanisole → 1-Fluoro-4-(isocyanomethyl)-2-methoxy-5-nitrobenzene

https://huagongshe.com/reaction/576583

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluoro-4-nitroanisoleHCID 223104—
反応物2-(4-Chlorophenoxy)acetonitrileHCID 306444—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylformamideHCID 6228—
生成物1-Fluoro-4-(isocyanomethyl)-2-methoxy-5-nitrobenzeneHCID 8671261924.4%

反応手順

Potassium t-butoxide (15.74 g, 140 mmol) in DMF (50 mL) was added to a solution of 2-fluoro-1-methoxy-4-nitrobenzene (12 g, 70.1 mmol) and 2-(4-chlorophenoxy)acetonitrile (11.75 g, 70.1 mmol) in DMF (100 mL) at −20° C. The reaction mixture was stirred for 1 h and then quenched with water. The aqueous layer was extracted with ethyl acetate. Organic layer was separated, washed with brine, dried over sodium sulphate, filtered and concentrated in vacuo. The crude product was purified by flash chromatography using 3% ethyl acetate in hexane to afford title compound (3.6 g, 23.21%) as a solid. 1H NMR (400 MHz, CDCl3): δ 8.05 (d, J=10.84 Hz, 1H), 7.27-7.23 (m, 1H), 4.28 (s, 2H), 4.05 (s, 3H); ESI-MS m/z=209 (M−H)−; LCMS Purity: 95%

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040517B2
出典データセットuspto-grants-2015_05
ORD IDord-86656cf8dfcf4b7886ed57f417020fc1
出典メモuspto-grants-2015_05