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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651003Generated: October 31, 2026

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

https://huagongshe.com/reaction/651003

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) and 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 numberUS06277873B1
Source datasetuspto-grants-2001_08
ORD IDord-235234aeedf84ebe8a6d780db2f9deb0
Source noteuspto-grants-2001_08