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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651387Generated: October 27, 2026

4-Bromophenacyl bromide → 4-(4-Bromo-phenyl)-2-(4-fluoro-phenyl)-thiazole

https://huagongshe.com/reaction/651387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromophenacyl bromideHCID 7454—
Reactant4-FluorothiobenzamideHCID 737223—
SolventEthanolHCID 702—
Product4-(4-Bromo-phenyl)-2-(4-fluoro-phenyl)-thiazoleHCID 11174998185.5%

Reaction Steps

To a solution of p-fluorothiobenzamide (0.39 g, 2.5 mmol) in 20 mL of abs. EtOH is added 2,4′-dibromoacetophenone (0.7 g, 2.5 mmol) all at once. The reaction mixture is stirred at room temperature for 3 hours and then chilled in ice bath. The precipitate is collected by filtration, washed with cold EtOH (5 ml×2) and dried in vacuum to give 2-(4′-fluorophenyl)-4-(4′-bromophenyl)thiazole as a white fluffy crystaline solid (1.55 g, 93%). mp.158-9° C. 1H NMR (CDCl3): δ 7.16 (t, 2H), 7.47 (s, 1H), 7.58 (d, 2H), 7.87 ()d, 2H), 8.02 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281217B1
Source datasetuspto-grants-2001_08
ORD IDord-ddf4d59357014a4196c1c000f7c3265a
Source noteuspto-grants-2001_08