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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095301Generated: October 31, 2026

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

https://huagongshe.com/reaction/1095301

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 60 F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138176B2
Source datasetuspto-grants-2012_03
ORD IDord-7a379bb01a704fa6a3c3b18e5063e3ca
Source noteuspto-grants-2012_03