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HRID 30761作成日:2026年10月26日

Ethanol → 2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethan-1-ol

https://huagongshe.com/reaction/30761

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物TetrahydrofuranHCID 8028—
反応物Ethyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetateHCID 3464653—
反応物Sodium borohydrideHCID 4311764—
溶媒WaterHCID 962—
生成物2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethan-1-olHCID 2313419298.5%

反応手順

Sodium borohydride (0.33 g) was added to a mixture of ethyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]-acetate (1.33 g), tetrahydrofuran (10 mL) and ethanol (10 mL). The mixture was stirred at room temperature for 4 hrs, and water was added. The resulting mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=2/1) to afford the title compound (1.13 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423185B2
出典データセットuspto-grants-2008_09
ORD IDord-bbf95566f52e4ad68e69211467a2c659
出典メモuspto-grants-2008_09