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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811052Generated: October 31, 2026

1-Bromo-2-fluoro-3-nitrobenzene → 3-Bromo-2-fluoroaniline

https://huagongshe.com/reaction/1811052

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-fluoro-3-nitrobenzeneHCID 40427446—
CatalystIronHCID 23925—
SolventAcetic acid ethanol waterHCID 86584229—
Product3-Bromo-2-fluoroanilineHCID 2234189193%

Reaction Steps

A solution of 1-bromo-2-fluoro-3-nitrobenzene (1.10 g, 5.00 mmol) in ethanol-acetic acid-water (2:2:1) (25 mL) was treated with iron powder (1.396 g, 25.0 mmol) and the mixture was heated at reflux for 1 h. The mixture was cooled to rt and filtered through a Celite pad. The filtrate was concentrated and the residue was partitioned between EtOAc and NaHCO3 (aq). The organic phase was washed with brine, dried and concentrated to provide 3-bromo-2-fluoroaniline as a brown oil (880 mg, 93%). 1H NMR (400 MHz, chloroform-d) δ 6.85-6.92 (1H, m), 6.80 (1H, td, J=8.0, 1.2 Hz), 6.66-6.73 (1H, m), 3.81 (2H, br. s.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362065B2
Source datasetuspto-grants-2013_01
ORD IDord-ccb6405c5cc54b75af38d057cf98e713
Source noteuspto-grants-2013_01