HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888743Generated: October 26, 2026
Imidazole → Methyl 2-{[tert-butyl(dimethyl)silyl]oxy}-4-{[4-(methoxymethoxy)phenyl]ethynyl}benzoate
https://huagongshe.com/reaction/1888743
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Methyl 4-iodosalicylate | HCID 11380407 | — |
| Reactant | 1-Ethynyl-4-(methoxymethoxy)benzene | HCID 22502995 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-{[tert-butyl(dimethyl)silyl]oxy}-4-{[4-(methoxymethoxy)phenyl]ethynyl}benzoate | HCID 58047299 | 84.4% |
Reaction Steps
To a solution of methyl 2-hydroxy-4-iodobenzoate (6.55 g, 23.6 mmol), 1-ethynyl-4-(methoxymethoxy)benzene (4.58 g, 28.3 mmol) and copper(I) iodide (450 mg, 2.36 mmol) in triethylamine (50 mL) was added bis(triphenylphosphine)palladium(II) chloride (1.66 mg, 2.36 mmol), and the mixture was stirred under an argon stream at room temperature for 30 min. The reaction mixture was diluted with ethyl acetate, and the mixture was washed with water, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was dissolved in DMF (30 mL). Imidazole (2.42 g, 35.4 mmol) and tert-butyl(chloro)dimethylsilane (4.27 g, 28.3 mmol) were added thereto, and the mixture was stirred at room temperature for 1.5 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed twice with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=19:1 to 3:2) to give the title compound (8.50 g, yield 84%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501804B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-c945331e8ff2433c95fa00b985d9ec22 |
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| Source note | uspto-grants-2013_08 |
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