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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467984Generated: October 30, 2026

Cesium carbonate → HCID 58216913, compound

https://huagongshe.com/reaction/467984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-Bromobenzyl cyanideHCID 29625—
ReactantHCID 178428694HCID 178428694—
CatalystCopper iodideHCID 83717—
ProductHCID 58216913HCID 58216913—

Reaction Conditions

Temperature120 °C

Reaction Steps

A round bottom flask was charged under inert atmosphere with copper iodide (760 mg, 4 mmol), cesium carbonate (3.91 g, 12 mmol) then dimethylformamide (20 mL), previously degassed, was added followed by 2-Bromophenylacetonitrile (519 μL, 4 mmol), 3-Methylpyrazole (3.32 mL, 40 mmol) and N—N′-dimethylethylenediamine (425.86 μL, 4 mmol). The reaction mixture was heated to 120° C. for 2.5 hours. After cooling the reaction mixture was filtered through a Celite pad that was rinsed with dimethylformamide. The volume was reduced under reduced pressure, saturated ammonium chloride aqueous solution was added and extracted with ethyl acetate. The organic phase was washed with saturated aqueous NH4Cl solution, brine then dried over Na2SO4 and the solvent was removed under reduced pressure. The crude product was purified by flash chromatography on SiO2 using cyclohexane/ethyl acetate mixture of increasing polarity (from 100% cyclohexane to 100% ethyl acetate) as eluent. The oil obtained was further purified by SPE Stratosphere “PL-THIOL MP” to completely remove copper salts. The title compound was obtained as a thick dark oil (300 mg, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623901B2
Source datasetuspto-grants-2014_01
ORD IDord-a40ad2e7a8094492b4bc218758d65f2b
Source noteuspto-grants-2014_01