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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360136Generated: October 29, 2026

4-Iodobenzonitrile → 4-[2-(1-trityl-1H-imidazol-4-ylmethoxy)acetyl]benzonitrile

https://huagongshe.com/reaction/1360136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodobenzonitrileHCID 76467—
ReactantN-methoxy-N-methyl-2-(1-trityl-1H-imidazol-4-ylmethoxy)acetamideHCID 86632953—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product4-[2-(1-trityl-1H-imidazol-4-ylmethoxy)acetyl]benzonitrileHCID 66782326—

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of 14 mmol of 4-iodobenzonitrile [3058-39-7] in 20 ml of tetrahydrofuran is cooled to −30° C., and 14.80 mmol of i-propylmagnesium chloride (2M in tetrahydrofuran) are added. The mixture is stirred at −30° C. for 60 minutes and a solution, precooled to −30° C., of 10.0 mmol of N-methoxy-N-methyl-2-(1-trityl-1H-imidazol-4-ylmethoxy)acetamide in 30 ml of tetrahydrofuran is added. The mixture is stirred at −30° C. for 30 minutes, and then the reaction mixture is warmed to room temperature and quenched with saturated aqueous ammonium chloride, solution. The phases are separated, and the aqueous phase is extracted with ethyl acetate (3×). The combined organic phases are washed with brine, dried with magnesium sulphate and evaporated. The title compound is identified from the residue on the basis of the Rf by flash chromatography (SiO2 60F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879847B2
Source datasetuspto-grants-2011_02
ORD IDord-c3e962acbe3745babacef3a6a7070b29
Source noteuspto-grants-2011_02