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HRID 39604Erstellt: 23. Oktober 2026
Pinacol → 2-(Chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
https://huagongshe.com/de/reaction/39604
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pinacol | HCID 6425 | — |
| Edukt | Chloroiodomethane | HCID 11644 | — |
| Edukt | Triisopropyl borate | HCID 21531 | — |
| Edukt | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 2-(Chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 11126810 | 81% |
Reaktionsschritte
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%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524946B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-9a7a9e92b21340fe8e2bf03088ad2df9 |
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| Quellennotiz | uspto-grants-2013_09 |
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