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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167334Generated: October 30, 2026

Hydroxylamine → HCID 59533941, compound

https://huagongshe.com/reaction/2167334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
Reactant4-[(Pyridin-2-yl)oxy]benzonitrileHCID 18525832—
SolventEthanolHCID 702—
ProductHCID 59533941HCID 59533941—

Reaction Steps

4-(Pyridin-2-yloxy)benzonitrile (701 mg, 3.57 mmol) was dissolved in ethanol (14.0 mL), and hydroxylamine (472 mg, 14.3 mmol) was added and the mixture was refluxed for 16 hours. The reaction was cooled to room temperature and then concentrated in vacuo to give the product as a yellow syrup and was taken to the next step without further purification (818 mg, 100%). 1H NMR (500 MHz, CDCL3) δ(ppm): 4.91 (2H, bs), 6.94 (1H, dt, J=8.4, 0.8 Hz), 7.02 (1H, ddd, J=7.2, 5.0, 0.8 Hz), 7.16 (2H, d, J=8.6 Hz), 7.66 (2H, d, J=8.6 Hz), 7.71 (1H, ddd, J=8.2, 7.2, 2.0 Hz), 8.21 (1H, ddd, J=5.0, 2.0, 0.8 Hz). 13C NMR (125 MHz, CDCL3) δ(ppm): 112.1 (CH), 119.1 (CH), 121.4 (CH), 127.6 (CH), 129.0, 139.8 (CH), 147.9 (CH), 152.4, 155.8, 163.4. MS (FAB+): 230 (MH+). HRMS for C12H11N3O2 (MH+): calculated: 230.0930; found 230.0934.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045442B2
Source datasetuspto-grants-2015_06
ORD IDord-05c5a7f94b12490181955175429d7166
Source noteuspto-grants-2015_06