Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651386Generated: October 27, 2026

2-Bromo-4'-methylacetophenone → 2-(4'-Fluorophenyl)-4-(p-tolyl)thiazole

https://huagongshe.com/reaction/651386

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4'-methylacetophenoneHCID 69272—
Reactant4-FluorothiobenzamideHCID 737223—
SolventEthanolHCID 702—
Product2-(4'-Fluorophenyl)-4-(p-tolyl)thiazoleHCID 1133470654%

Reaction Steps

To a solution of the crude product of 4-fluorothiobenzamide (2.0 g, 12.9 mmol) in EtOH (30 ml) is added 2-bromo-4′methylacetophenone (2.75 g, 12.9 mmol). The mixture is heated to reflux for 24 hours. The course of the reaction is followed by thin layer chromatography. Upon completion of the reaction the solution is cooled to room temperature and the white precipitate filtered and dried under vacuum to yield 2- (4′-fluorophenyl)-4- (p-tolyl) thiazole (1.54 g, 54%). 1H NMR (DMSOd6): δ 2.35 (s, 1H), 7.28 (d, 2H), 7.38 (t, 2H), 7.94 (d, 2H), 8.08 (dd, 2H), 8.11 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281217B1
Source datasetuspto-grants-2001_08
ORD IDord-7fb5b984cece48ec803bc974633dda1e
Source noteuspto-grants-2001_08