HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159348Generated: October 31, 2026
2,5-Difluoronitrobenzene → HCID 24890306, compound
https://huagongshe.com/reaction/1159348
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,5-Difluoronitrobenzene | HCID 67767 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 57444205 | HCID 57444205 | — |
| Product | HCID 24890306 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812050B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-50380c9d0b1f47f2be7ba0d36713df86 |
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| Source note | uspto-grants-2010_10 |
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