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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497301Generated: October 29, 2026

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

https://huagongshe.com/reaction/497301

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 numberUS06949536B2
Source datasetuspto-grants-2005_09
ORD IDord-b715ebddeb2347c0afb4846d30c2d4ab
Source noteuspto-grants-2005_09