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Imidazole → 5-Iodo-2-triisopropylsilanyloxy-benzoic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Imidazole | HCID 795 | — |
| 反応物 | Triisopropylsilyl chloride | HCID 139400 | — |
| 反応物 | Methyl 5-Iodosalicylate | HCID 248910 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 5-Iodo-2-triisopropylsilanyloxy-benzoic acid methyl ester | HCID 123371874 | 92.1% |
反応手順
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+].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09440974B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-d2b657b18bee487ca61d7522a786f771 |
| 出典メモ | uspto-grants-2016_09 |