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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651395Generated: October 27, 2026

N-bromobutanimide → 5-(4-Fluorophenyl)-3-(p-bromomethylphenyl)-1,2,4-thiadiazole

https://huagongshe.com/reaction/651395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-(4'-Fluorophenyl)-3-(p-tolyl)-1,2,4-thiadiazoleHCID 22611069—
SolventCarbon TetrachlorideHCID 5943—
Product5-(4-Fluorophenyl)-3-(p-bromomethylphenyl)-1,2,4-thiadiazoleHCID 22611062106.8%

Reaction Steps

To a solution of 5-(4′-fluorophenyl)-3-(p-tolyl)-1,2,4-thiadiazole (0.16 g, 0.59 mmol) in CCl4 (20 ml) is added NBS (0.11 g, 0.59 mmol) and the mixture is heated to reflux for 36 hours. The mixture is cooled to room temperature and filtered through celite. The mother liquor is concentrated. The residue is taken up in chloroform (30 ml) amd washed with water (30 ml). The organic layer is dried over MgSO4 and concentrated to yield 5-(4′-fluorophenyl)-3-(p-bromomethylphenyl)-1,2,4-thiadiazole, (0.22 g) as crude product which is used as is without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281217B1
Source datasetuspto-grants-2001_08
ORD IDord-caae91279d384e8a8acde34588ff1039
Source noteuspto-grants-2001_08