Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908581Generated: October 30, 2026

Potassium Cyanide → HCID 11998318, compound

https://huagongshe.com/reaction/908581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantTributyltin ChlorideHCID 15096—
ReactantHCID 86637146HCID 86637146—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventAcetonitrileHCID 6342—
SolventHeptaneHCID 8900—
ProductHCID 11998318HCID 11998318—

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Bromo-6-(3-pyridin-3-yl-[1,2,4]oxadiazol-5-yl)-pyridine (250 mg, 0.83 mmol) and 80 mg of potassium cyanide (1.24 mmol) in 15 ml of acetonitrile was degassed three times (vacuum/nitrogene), added a solution of 24 μl Tributyltin chloride (1 μmol) in heptane, 2.3 mg of bis-(diphenylphosphino)ferrocene (4.1 μmol) and 4 mg of bispalladium tris(dibenzylidene acetone) (4.1 μmol) were added. The suspension was degassed three times and stirred at ambident temperature for 30 minutes. The mixture was degassed again and heated at 80° C. for 17 hours. The reaction mixture concentrated, residue was diluted with ethyl acetate and washed with water. The organic layer was dried with sodium sulphate, concentrated, and purified by column chromatography over silica gel using 20% ethyl acetate in petroleum ether, Yield 80 mg. Mp 201-203° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017631B2
Source datasetuspto-grants-2011_09
ORD IDord-e5015aa5a6ba470081a7c22f30662580
Source noteuspto-grants-2011_09