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HRID 337841作成日:2026年10月26日

Water → 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,4-dioxaspiro[4.5]dec-6-ene

https://huagongshe.com/reaction/337841

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
反応物6-Iodo-1,4-dioxaspiro[4.5]dec-6-eneHCID 14631807—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,4-dioxaspiro[4.5]dec-6-eneHCID 8996345156%

反応条件

温度-78 °C

反応手順

To a solution of 6-iodo-1,4-dioxaspiro[4.5]dec-6-ene (Synlett, 2008, 1086-1090; 2.70 g, 10.2 mmol) in THF (30 mL), butyl lithium (1.65 M solution in hexane; 6.7 mL, 11.1 mmol) was added at −78° C. The reaction solution was stirred at −78° C. for 1 hour. Then, 4,4,5,5-tetramethyl-2-(propan-2-yloxy)-1,3,2-dioxaborolane (4.0 mL, 19.8 mmol) was added thereto, and the mixture was stirred at −78° C. for 2 hours. To the reaction solution, water (50 mL) was added, followed by extraction with ethyl acetate (50 mL). The thus obtained organic layer was dried over anhydrous sodium sulfate. After vacuum concentration, the residue was purified with silica gel chromatography (hexane/ethyl acetate=9:1) to yield the title compound (1.52 g, 56%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889741B2
出典データセットuspto-grants-2014_11
ORD IDord-beb2518ec90842ddbc94d74f4d5a8283
出典メモuspto-grants-2014_11