Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621838Generated: November 1, 2026

Ammonium Chloride → 7-Bromo-5-fluoroquinoline

https://huagongshe.com/reaction/1621838

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 numberUS08772480B2
Source datasetuspto-grants-2014_07
ORD IDord-dde9d5f7e0ed4d3abb2c7dd9ce3a7ac1
Source noteuspto-grants-2014_07