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HRID 78263生成日期:2026年10月23日

氯甲基甲基醚 → 1-Bromo-3-[(methoxymethoxy)methyl]benzene

https://huagongshe.com/zh-CN/reaction/78263

反应方程式

参与物

角色名称HCID投料
反应物氯甲基甲基醚HCID 7864—
反应物氢化钠HCID 24758—
反应物3-溴苯甲醇HCID 85141—
溶剂四氢呋喃HCID 8028—
产物1-Bromo-3-[(methoxymethoxy)methyl]benzeneHCID 1144757883%

反应条件

温度60 °C

反应步骤

To a tetrahydrofuran (100 mL) solution of 3-bromobenzyl alcohol (10 g, 54 mmol) was added sodium hydride (2.3 g, 98 mmol, 60% in oil) at room temperature. Then, chloromethyl methyl ether (5.2 g, 64 mmol) was added to this suspension, which was stirred for 15 minutes at 60° C. This mixture was partitioned into ethyl acetate and water. The organic layer was separated and concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=8:1) to obtain the title compound (10 g, 83%).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08841327B2
来源数据集uspto-grants-2014_09
ORD IDord-4203a6b99c9c41c7b61a2107c2ecb1da
来源说明uspto-grants-2014_09