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HRID 640494作成日:2026年10月25日

Dibromomethane → 2-(Bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

https://huagongshe.com/reaction/640494

反応式

関与物質

役割名称HCID仕込み量
反応物DibromomethaneHCID 3024—
反応物Methanesulfonic AcidHCID 6395—
反応物PinacolHCID 6425—
反応物Triisopropyl borateHCID 21531—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2-(Bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 1095511068%

反応条件

温度0 °C

反応手順

To a mixture of triisopropyl borate (20 g, 110 mmol), dibromomethane (8.6 mL, 120 mmol), and tetrahydrofuran (150 mL) was added dropwise n-butyl lithium (2.6 M n-hexane solution, 39 mL, 100 mmol) over a period of 1.5 hours at −78° C., and then the reaction mixture was stirred for 1.5 hours at the same temperature. This mixture was then stirred for 2 hours at room temperature, after which it was cooled to 0° C., methanesulfonic acid (6.5 mL, 100 mmol) was added to the reaction mixture, and then the reaction mixture was stirred for 1 hour at room temperature. The mixture was cooled to 0° C., pinacol (12 g, 100 mmol) was added to the reaction mixture, and the reaction mixture was then stirred for 1 hour at room temperature. The reaction mixture was concentrated under a reduced pressure, after which the residue thus obtained was distilled under a reduced pressure (74-76° C., 8 mmHg) to obtain the title compound (16 g, 68%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07691882B2
出典データセットuspto-grants-2010_04
ORD IDord-bd861c5ec4514996aed22a230e198774
出典メモuspto-grants-2010_04