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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528337Generated: October 26, 2026

Potassium Iodide → HCID 140660333, compound

https://huagongshe.com/reaction/1528337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
ReactantN-Hydroxybenzimidoyl cyanideHCID 5464219—
Reactanttert-Butyl (6-(chloromethyl)pyridin-2-yl)carbamateHCID 21851761—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHCID 140660333HCID 14066033380%

Reaction Steps

To a solution of (2Z)-(hydroxyimino)(phenyl)acetonitrile (2.5 g, 17.10 mmol, 1 eq.) in 100 ml of acetonitrile and 10 ml DMF was added tert-butyl [6-(chloromethyl)pyridin-2-yl]carbamate (4.15 g, 17.10 mmol, 1 eq.) followed by potassium iodide (283 mg, 1.71 mmol, 0.1 eq.) and caesium carbonate (8.36 g, 25.65 mmol, 1.5 eq.). The reaction was stirred overnight at room temperature. The solvent was than evaporated and the residue dissolved in EtOAc (100 ml). The organic layer was washed with H2O and dried over MgSO4 then concentrated. tert-butyl {6-[({[(Z)-cyano(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate (5.39 g, 80% yield, only 1 oxime isomer) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090600B2
Source datasetuspto-grants-2015_07
ORD IDord-80dfea344039410cbb2dbd8935c859b4
Source noteuspto-grants-2015_07