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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559875Generated: October 25, 2026

2-Aminothiazole → 5-Fluoro-2-(2-trifluromethylphenoxy)-1-nitrobenzene

https://huagongshe.com/reaction/559875

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant2,5-DifluoronitrobenzeneHCID 67767—
Reactant2-TrifluoromethylphenolHCID 67958—
Reactant2-(2-Trifluoromethylphenoxy)-5-fluoroanilineHCID 28412097—
Productn-[5-Fluoro-2-(2-trifluoromethylphenoxy)phenyl]-n'-(thiazol-2-yl)ureaHCID 5973296474%
Product5-Fluoro-2-(2-trifluromethylphenoxy)-1-nitrobenzeneHCID 6699899278%

Reaction Steps

5-Fluoro-2-(2-trifluoromethylphenoxy)-1-nitrobenzene (1.17 g, 78%) was prepared from 2-hydroxybenzotrifluoride (0.89 g, 5.5 mmol) and 2,5-difluoro-1-nitrobenzene (0.8 g, 5.0 mmol) following the general procedure A. This compound was reduced to 5-fluoro-2-(2-trifluoromethylphenoxy)-aniline (0.65 g, 62%) following the general procedure B. N-[5-Fluoro-2-(2-trifluoromethylphenoxy)phenyl]-N′-(thiazol-2-yl)urea (146 mg, 74%) was prepared from 2-(2-trifluoromethylphenoxy)-5-fluoroaniline (135 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063081B2
Source datasetuspto-grants-2011_11
ORD IDord-68b1e535726f4ac4b06f0e6085c128f1
Source noteuspto-grants-2011_11