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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159348Generated: October 31, 2026

2,5-Difluoronitrobenzene → HCID 24890306, compound

https://huagongshe.com/reaction/1159348

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DifluoronitrobenzeneHCID 67767—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 57444205HCID 57444205—
ProductHCID 24890306HCID 24890306—

Reaction Steps

3-Fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin can be prepared according to the teachings provided herein and the knowledge in the art. Briefly, treating 5-(2,2,2-trifluoroethoxy)-2-mercaptophenol with base followed by addition of 1,4-difluoro-2-nitrobenzene can afford 3-fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin. For example, 5-(2,2,2-trifluoroethoxy)-2-mercaptophenol can be combined with potassium tert-butoxide followed by combination with 1,4-difluoro-2-nitrobenzene which upon heating can afford 3-fluoro-7-(2,2,2-trifluoroethoxy)phenoxathiin. In an exemplary embodiment, the solvent used to dissolve potassium tert-butoxide and 1,4-difluoro-2-nitrobenzene can be anhydrous N,N-dimethylformamide. For example, 5-(2,2,2-trifluoroethoxy)-2-mercaptophenol dissolved in a THF/MTBE mixture can be added to potassium tert-butoxide in N,N-dimethylformamide; subsequent to their combination, under the conditions disclosed herein, the mixture can then be treated with 1,4-difluoro-2-nitrobenzene dissolved in N,N-dimethylformamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812050B2
Source datasetuspto-grants-2010_10
ORD IDord-50380c9d0b1f47f2be7ba0d36713df86
Source noteuspto-grants-2010_10