HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112167Generated: November 1, 2026
Potassium Carbonate → 5-Fluoro-2-(3-methyl-benzo[d]isoxazol-6-yloxy)-benzonitrile
https://huagongshe.com/reaction/2112167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Difluorobenzonitrile | HCID 123558 | — |
| Reactant | 3-Methyl-1,2-benzisoxazol-6-ol | HCID 135497890 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 5-Fluoro-2-(3-methyl-benzo[d]isoxazol-6-yloxy)-benzonitrile | HCID 57484118 | 58% |
Reaction Steps
3-Methyl-benzo[d]isoxazol-6-ol (1v) (reference for synthesis, see Indian J. Chem. Sect.B; 19:571-575 (1980)) (1.58 g, 10.6 mmol) and 2,5-difluoro-benzonitrile (2v) (1.47 g, 10.6 mmol) were combined with potassium carbonate (1.46 g. 10.6 mmol) in 15 mL of dry DMA. The reaction was heated in a 100° C. bath for 6 hours. The reaction was cooled and diluted with EtOAc (200 mL) and washed three times with water, NH4Cl, NaHCO3, and brine. The organic solution was dried over MgSO4 and concentrated. The crude residue was purified by column chromatography (silica, 70-80% CH2Cl2/hexane) to provide compound (3v) (1.65 g, 58% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07521447B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-d16d8e781f9a4af7b46fe05f342307d0 |
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| Source note | uspto-grants-2009_04 |
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