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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Iodobenzonitrile | HCID 76467 | — |
| Reactant | N-methoxy-N-methyl-2-(1-trityl-1H-imidazol-4-ylmethoxy)acetamide | HCID 86632953 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[2-(1-trityl-1H-imidazol-4-ylmethoxy)acetyl]benzonitrile | HCID 66782326 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879847B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-c3e962acbe3745babacef3a6a7070b29 |
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| Source note | uspto-grants-2011_02 |
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