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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54313Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/54313

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktN-bromobutanimideHCID 67184—
Edukt4-Fluoro-2-nitroanilineHCID 67769—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Bromo-4-fluoro-6-nitroanilineHCID 292004—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05622952
Quelldatensatzuspto-grants-1997_04
ORD IDord-2c127c3d76424c8c9494c46b0a7809bd
Quellennotizuspto-grants-1997_04