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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086670Generated: November 2, 2026

Formamide → 4-(4-Bromophenyl)thiazole

https://huagongshe.com/reaction/2086670

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 numberUS06727238B2
Source datasetuspto-grants-2004_04
ORD IDord-2fe3d745383c43d2be4e5bb8200e01eb
Source noteuspto-grants-2004_04