HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754419Generated: October 28, 2026
2-Fluoro-5-nitrobenzonitrile → HCID 86704472, compound
https://huagongshe.com/reaction/1754419
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoro-5-nitrobenzonitrile | HCID 519417 | — |
| Reactant | Oxetan-3-ol | HCID 9942117 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86704472 | HCID 86704472 | 90% |
Reaction Steps
3-Hydroxy oxetane (370 mg, 5 mmol, 2 equiv) in THF (15 ml) under argon gas, was cooled to 0° C. Potassium tert-butoxide (617 mg, 5.5 mmol, 2.2 equiv) was added in one portion, and the reaction mixture was stirred for 20 minutes at 0° C. Then 2-fluoro-5-nitrobenzonitrile (415 mg, 2.5 mmol, 1 equiv) was added in one portion, and the reaction mixture was stirred for 10 minutes at 0° C. and allowed to warm up to ambient temperature over 1 hour. The reaction mixture was concentrated, and the residue was taken in DCM and water. The layers were separated, and the organic layer was washed with water (×2), dried over Na2SO4, filtered, and concentrated to provide 5-nitro-2-(oxetan-3-yloxy)benzonitrile (495 mg, 90%) as a brown-yellow solid that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169249B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-f2733f02c78b48fcb978163d2b5a2d15 |
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| Source note | uspto-grants-2015_10 |
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