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HRID 39604作成日:2026年10月23日

Pinacol → 2-(Chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

https://huagongshe.com/ja/reaction/39604

反応式

関与物質

役割名称HCID仕込み量
反応物PinacolHCID 6425—
反応物ChloroiodomethaneHCID 11644—
反応物Triisopropyl borateHCID 21531—
反応物Hydrogen chloride-ethyl acetateHCID 21866389—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物2-(Chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 1112681081%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524946B2
出典データセットuspto-grants-2013_09
ORD IDord-9a7a9e92b21340fe8e2bf03088ad2df9
出典メモuspto-grants-2013_09