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HRID 241476生成日期:2026年10月23日

四氢呋喃 → 2,3-二氟苯硼酸

https://huagongshe.com/zh-CN/reaction/241476

反应方程式

参与物

角色名称HCID投料
反应物四氢呋喃HCID 8028—
反应物1,2-二氟苯HCID 9706—
反应物硼酸三丙酯HCID 12711—
反应物正丁基锂HCID 178418339—
溶剂正己烷HCID 8058—
产物2,3-二氟苯硼酸HCID 273433385%

反应条件

温度-78 °C

反应步骤

1,2-Difluorobenzene (40 g, 0.35 mol) and dry tetrahydrofurane (400 ml) were placed in 1 L flask equipped with mechanical stirrer, nitrogen inlet and outlet, pressure-equilibrated dropping funnel and thermometer. The reaction flask was flushed with nitrogen and minor flow was held during whole reaction time. The mixture was cooled down to −78° C. with dry ice/acetone bath and 2.5 mol/L hexane solution of n-butyllithium (140 ml; 0.35 mol) was added dropwise, keeping the reaction temperature below −70° C. After addition of all butyllithium solution the mixture was stirred at −78° C. for 2 h and then tripropylborate (66 g, 0.35 mol) was added dropwise keeping the reaction temperature below −70° C. After addition of tripropyl borate the cooling bath was removed and the reaction mixture continuously stirred to reach the room temperature then the solvents were evaporated. The thick liquid residue was acidified and then propanol was evaporated and the remaining solid was filtered off, washed out with hexane and recrystalized from water. The white crystalline product 47 g was obtained, with 85% of theor. yield.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08652353B2
来源数据集uspto-grants-2014_02
ORD IDord-1c217f3a325e4b0da3dc4b1b100c870b
来源说明uspto-grants-2014_02