関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pinacol | HCID 6425 | — |
| 反応物 | Chloroiodomethane | HCID 11644 | — |
| 反応物 | Triisopropyl borate | HCID 21531 | — |
| 反応物 | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 2-(Chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 11126810 | 81% |
反応手順
To the mixture of triisopropyl borate (15 ml, 65 mmol), chloroiodomethane (13 g, 72 mmol), and tetrahydrofuran (78 ml), n-butyllithium (a 1.6 M n-hexane solution, 41 ml, 65 mmol) was added dropwise at −78° C. (an outer temperature) for 20 min, and then the obtained mixture was stirred at room temperature for 2.5 hours. The reaction mixture was cooled to 0° C. (an outer temperature), and a 4 N hydrochloric acid-ethyl acetate solution was added dropwise thereto at the same temperature until the reaction mixture became neutral. At the same temperature, pinacol (7.7 g, 65 mmol) was added to the reaction mixture, and then the reaction mixture was stirred at room temperature for 40 min. The solvents were evaporated under reduced pressure, and then the obtained residue was distilled under reduced pressure (63-70° C., 11 mmHg), thereby obtaining the entitled compound (9.2 g, 52 mmol, 81%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08524946B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-9a7a9e92b21340fe8e2bf03088ad2df9 |
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| 出典メモ | uspto-grants-2013_09 |
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