Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068495Generated: October 26, 2026

1,1-Dibromoethane → 1-Trityl-4-(4-cyanobenzyl)imidazole

https://huagongshe.com/reaction/1068495

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DibromoethaneHCID 11201—
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
Reactant4-Iodo-1-tritylimidazoleHCID 618252—
CatalystZincHCID 23994—
Catalystbis(triphenylphosphine) NickelHCID 57357981—
SolventTetrahydrofuranHCID 8028—
Product1-Trityl-4-(4-cyanobenzyl)imidazoleHCID 15837533—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a suspension of activated zinc dust (3.57 g, 54.98 mmol) in THF (50 mL) was added dibromoethane (0.315 mL, 3.60 mmol) and the reaction stirred under argon for 45 minutes, at 20° C. The suspension was cooled to 0° C. and a-bromo-p-tolunitrile (9.33 g, 47.6 mmol) in THF (100 mL) was added dropwise over a period of 10 minutes. The reaction was then allowed to stir at 20° C. for 6 hours and bis(triphenylphosphine) Nickel II chloride (2.40 g, 3.64 mmol) and 4-iodo-1-tritylimidazole (15.95 g, 36.6 mmol, S. V. Ley, et al., J. Org. Chem. 56, 5739(1991)) were added in one portion. The resulting mixture was stirred 16 hours at 20° C. and then quenched by addition of saturated NH4Cl solution (100 mL) and the mixture stirred for 2 hours. Saturated aq. NaHCO3 solution was added to give a pH of 8 and the solution was extracted with EtOAc (2×250 mL), dried (MgSO4) and the solvent evaporated in vacuo. The residue was chromatographed (Silica gel, 0-20% EtOAc in CH2Cl2) to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248756B1
Source datasetuspto-grants-2001_06
ORD IDord-9041a4c2490f42829de0651b0f7a2a7e
Source noteuspto-grants-2001_06