HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443302Generated: October 26, 2026
1,1-Dibromoethane → 1-Trityl-4-(4-cyanobenzyl)imidazole
https://huagongshe.com/reaction/443302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | 4-(Bromomethyl)benzonitrile | HCID 86996 | — |
| Reactant | 4-Iodo-1-tritylimidazole | HCID 618252 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Catalyst | bis(triphenylphosphine) Nickel | HCID 57357981 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Trityl-4-(4-cyanobenzyl)imidazole | HCID 15837533 | — |
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 α-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05891889 |
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| Source dataset | uspto-grants-1999_04 |
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| ORD ID | ord-b785ab5f372e4112b3ba055991d9440a |
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| Source note | uspto-grants-1999_04 |
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