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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-5-nitrobenzonitrileHCID 519417—
ReactantOxetan-3-olHCID 9942117—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86704472HCID 8670447290%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169249B2
Source datasetuspto-grants-2015_10
ORD IDord-f2733f02c78b48fcb978163d2b5a2d15
Source noteuspto-grants-2015_10