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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510191Generated: November 3, 2026

Chlorobenzene → Undecane

https://huagongshe.com/reaction/1510191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantPotassium sodium tartarateHCID 9855836—
Reactant1,3-BIS(2,6-DIISOPROPYLPHENYL)imidazoLIDINIUM-CHLORIDEHCID 18454782—
ReactantHCID 178418370HCID 178418370—
SolventTetrahydrofuranHCID 8028—
ProductUndecaneHCID 1425791%

Reaction Steps

Chlorobenzene (45.0 mg, 0.4 mmol) and a THF solution of p-tolylmagnesium bromide (0.98 mL, 1.02 M, 1.0 mmol) was added to CoF2.4H2O (3.38 mg, 0.02 mmol), and 1,3-bis(2,6-diisopropylphenyl)imidazolinium chloride (25.6 mg, 0.06 mmol) at 0° C. under argon atmosphere. The mixture was reacted at 60° C. for 24 hours. After cooled to the ambient temperature, 1.0 mL of saturated sodium potassium tartrate aqueous solution was added to the reaction mixture. The water layer was extracted five times using Et2O. The total organic extract was filtrated by Florisil pad (100-200 mesh, Nacalai Tesque, Inc.). As the internal standard, gas chromatographic analysis was performed using undecane (42.2 μL, 0.2 mmol) (yield=91%). After removing the solvent under reduced pressure, the crude product was purified by silica gel chromatography (pentane), thereby obtaining the above compound, which was a colorless liquid (0.059 g, yield=88%, purity=>99% (GC analysis)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211820B2
Source datasetuspto-grants-2012_07
ORD IDord-cf6ccc310f674338801161aea25da523
Source noteuspto-grants-2012_07