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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086745Generated: October 30, 2026

Formamide → 2-Fluoro-4-(thiazol-4-yl)phenol

https://huagongshe.com/reaction/2086745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantMethanethioamideHCID 3005587—
Reactant2-Bromo-1-(3-fluoro-4-hydroxyphenyl)ethan-1-oneHCID 17923530—
Solvent1,4-DioxaneHCID 31275—
Product2-Fluoro-4-(thiazol-4-yl)phenolHCID 2231692283%

Reaction Steps

To a stirred solution of phosphorus pentasulfide (8.6 g, 19.3 mmol) in dioxane (53 ml) was added formamide (5.2 g, 115.5 mmol), and the mixture was heated at reflux temperature for 2 hours. The mixture was cooled down to room temperature, and the solution was decanted away from solids. To a stirred solution of 2-bromo-1-(3-fluoro-4-hydroxyphenyl)-1-ethanone (3.02 g, 12.98 mmol) in dioxane (50 ml) was added the thioformamide solution, and the mixture was heated at reflux temperature for 6 hours. The mixture was cooled down to room temperature, and made basic by addition of 0.5M NaOH aqueous solution. The whole was extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate-hexane (1:3) to give title compound (2.11 g, 83% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727238B2
Source datasetuspto-grants-2004_04
ORD IDord-e47de7ac2fc742619e5fe700be352675
Source noteuspto-grants-2004_04