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HRID 54313作成日:2026年10月25日

Water → 2-Bromo-4-fluoro-6-nitroaniline

https://huagongshe.com/reaction/54313

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物N-bromobutanimideHCID 67184—
反応物4-Fluoro-2-nitroanilineHCID 67769—
溶媒DimethylformamideHCID 6228—
生成物2-Bromo-4-fluoro-6-nitroanilineHCID 292004—

反応手順

6-Bromo-4-fluoro-2-nitroaniline was prepared using an adaptation of the method of Mitchell et al., J. Org. Chem. 44:4733 (1979). To a solution of 4-fluoro-2-nitroaniline (500 mg, 3.2 mmol) in dry DMF (16 mL) under N2 was added dropwise a solution of N-bromosuccinimide (570 mg, 3.2 mmol) in dry DMF (16 mL). The reaction was allowed to stir 24 h. The solution was then poured into 100mL H2O and this aqueous phase extracted with 4×25 mL CH2Cl2. The combined organic phases were washed with 3×4 mL H2O and dried (MgSO4). The MgSO4 was vacuum filtered and the solvent rotary evaporated to yield a brown oil which crystallized on standing. 642 mg (85.4%). 1H NMR (CDCl3) δ6.51 (br s, 2H NH2), 7.58 (dd, JH4-3 =3 Hz, JH4-F =6.5 Hz, H-4), 7.92 (dd, JH3-4 =3 Hz, JH3-F =8.7 Hz, H-3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622952
出典データセットuspto-grants-1997_04
ORD IDord-2c127c3d76424c8c9494c46b0a7809bd
出典メモuspto-grants-1997_04