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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1812246Generated: November 1, 2026

Ammonium Chloride → 7-Bromo-5-fluoroquinoline

https://huagongshe.com/reaction/1812246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(E)-3-(4-bromo-2-fluoro-6-nitrophenyl)acrylaldehydeHCID 86647069—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product7-Bromo-5-fluoroquinolineHCID 6660038555.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

A glass microwave reaction vessel was charged with (E)-3-(4-bromo-2-fluoro-6-nitrophenyl)acrylaldehyde (35 mg, 0.128 mmol), iron powder (0.018 mL, 2.55 mmol, Aldrich) and ammonium chloride (6.83 mg, 0.128 mmol, Aldrich) in ethanol (1 mL). The reaction mixture was stirred and heated in an Emrys Optimizer microwave reactor (Personal Chemistry, Biotage AB, Inc., Upssala, Sweden) at 120° C. for 5 min. The mixture was filtered through a pad of Celite® (diatomaceous earth), washed with EtOAc. The solvent was removed in vacuo and the residue was purified by silica gel chromatography eluting with 20% EtOAc/hexanes to give 7-bromo-5-fluoroquinoline (16 mg, 0.071 mmol, 55.4% yield). 1H NMR (300 MHz, CDCl3) δ 7.20-7.34 (m, 1H) 7.59-7.74 (m, 1H) 7.90 (d, J=8.48 Hz, 1H) 8.58 (d, J=1.61 Hz, 1H) 8.95 (d, J=2.34 Hz, 1H). m/z (ESI, +ve ion) 227.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-a21acfe641be434bb47da03342938467
Source noteuspto-grants-2013_01