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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497221Generated: October 30, 2026

Formamide → 4-(4-Bromophenyl)thiazole

https://huagongshe.com/reaction/497221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
Reactant4-Bromophenacyl bromideHCID 7454—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantMethanethioamideHCID 3005587—
Solvent1,4-DioxaneHCID 31275—
Product4-(4-Bromophenyl)thiazoleHCID 440413895%

Reaction Steps

To a stirred solution of phosphorus pentasulfide (24.5 g, 55 mmol) in dioxane (250 ml) was added formamide (28.4 g, 630 mmol), and the mixture was heated at reflux temperature for 2 hours. The reaction mixture was cooled down to room temperature, and the solution was decanted away from solids. To a stirred solution of 2,4′-dibromoacetophenone (15 g, 54 mmol) in dioxane (100 ml) was added the thioformamide solution, and the mixture was heated at reflux temperature for 6 hours. The reaction mixture was cooled down to room temperature, and made basic by addition of 2N NaOH aqueous solution. The whole was extracted with diethyl ether. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with CH2Cl2 to give title compound (12.3 g, 95% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949536B2
Source datasetuspto-grants-2005_09
ORD IDord-a1bae95be9284c5b83dee0f2d7b8a7d2
Source noteuspto-grants-2005_09