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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226840Generated: November 2, 2026

2-Bromobenzonitrile → HCID 18963827, compound

https://huagongshe.com/reaction/2226840

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromobenzonitrileHCID 16272—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18963827HCID 18963827114%

Reaction Conditions

Temperature-78 °C

Reaction Steps

The title D compound (1.99 g, 9.00 mmol) was dissolved in 10 mL of freshly distilled tetrahydrofuran, cooled to -78° C. and n-butyllithium (2.23M in hexane, 4.24 mL, 9.45 mmol) was added dropwise over 10 minutes. Upon complete addition the reaction was cloudy, bright yellow. After stirring 40 minutes, zinc chloride (1.0M in ether, 9.45 mL, 9.45 mmol) was added and the reaction mixture turned to clear pale yellow. The reaction was stirred 30 minutes, then the cold bath was removed and the reaction stirred an additional 30 minutes before 2-bromobenzonitrile (1.64 g, 9.45 mmol) and tetrakis(triphenylphosphine)palladium(O) (520 mg, 0.45 mmol) were added. After stirring 22 hours at 55° C., the reaction mixture was adsorbed on 10 g of silica gel and purified by flash chromatography (170 g silica gel; 30% toluene, hexane) to yield 1.31 g (60%) of the product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350752
Source datasetuspto-grants-1994_09
ORD IDord-700b42dd6ae54680b2dccba366454f52
Source noteuspto-grants-1994_09