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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176355Generated: October 29, 2026

Ethanol → HCID 57437658, compound

https://huagongshe.com/reaction/2176355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(1,3,2-Dioxaborinan-2-yl)benzonitrileHCID 3529602—
Reactant2-Bromo-4-butylbenzenamineHCID 19381134—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 57437658HCID 5743765865.9%

Reaction Steps

20.0 g (87.7 mmol) 2-(1,3,2-dioxaborinan-2-yl)benzonitrile, 13.7 g (73.1 mmol) 2-bromo-4-butylaniline, 1.70 g (1.46 mmol) tetrakis(triphenylphosphine)palladium(0), and 27.2 g (198 mmol) potassium carbonate where refluxed in 400 mL toluene and 200 mL ethanol under N2 atmosphere for 20 h. HPLC and TLC revealed almost complete consumption of the aniline. An additional 1.8 g 2-(1,3,2-dioxaborinan-2-yl)benzonitrile was added and refluxed continued for an additional 18 h. The reaction mixture was cooled and passed through a filter. The solids were washed with ethyl acetate to remove organics from the collected base. The filtrate was then evaporated down and dried on silica. The sample was purified using silica gel chromatography with 100% ethyl acetate as the eluent. The product fractions were then evaporated down to a minimal amount and the product recrystallized from EtOAc/hexanes to give 12.0 g of the title compound as light yellow solids (65.9% yield, GC-MS confirmed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09065063B2
Source datasetuspto-grants-2015_06
ORD IDord-a7626d993bf14ac1918a5bd16fc5ca8f
Source noteuspto-grants-2015_06