HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 5-Iodo-2-triisopropylsilanyloxy-benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Triisopropylsilyl chloride | HCID 139400 | — |
| Reactant | Methyl 5-Iodosalicylate | HCID 248910 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Iodo-2-triisopropylsilanyloxy-benzoic acid methyl ester | HCID 123371874 | 92.1% |
Reaction Steps
A solution of methyl 5-iodosalicylate (2.00 g, 7.20 mmol) in DMF (20 mL) was treated with imidazole (1.22 g, 18.0 mmol) then chlorotriisopropylsilane (1.85 mL, 8.60 mmol). The mixture was stirred at RT for 18 h. The mixture was evaporated in vacuo and the residue was partitioned between EtOAc and water. The aqueous layer was then extracted with EtOAc (2×). The combined organic layers were washed with a 10% aqueous citric acid solution, 1N aqueous NaOH solution and brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue was purified by FCC, using 0-10% EtOAc in cyclohexane, to give the title compound as a colorless oil (2.88 g, 92%). LCMS (Method 3): Rt 5.72 min, m/z 435 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09440974B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-d2b657b18bee487ca61d7522a786f771 |
| Source note | uspto-grants-2016_09 |