反应 #4084274
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1c4d2ee9c9804bc2ae3b03e7907aaeef暂无可渲染的结构数据
BrC1C=CC=C(C=1OC)Br产品信息
2,6-二溴苯甲醚(CAS 38603-09-7)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
可能的应用方向
仅供专业研发与工业用途
数据库编号 181584
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1c4d2ee9c9804bc2ae3b03e7907aaeef反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-07fcf513449d4b0eab38bd2631d7c44e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-265341a2180248ce9e84b4d29913b944反应条件: temp:40.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a THF solution of 2,6-dibromoanisole (10 g, 37.6 mmol) was added Mg (0.90 g, 37.6 mmol), and the mixture was heated and stirred at 40° C. Under ice-cooling, n-heptanal (47.2 g, 41.3 mmol) was added dropwise. Aqueous hydrochloric acid solution was added to the reaction mixture, this was extracted with ethyl acetate, and the solvent was distilled off to obtain 8.95 g of a compound (1). the mixture was heated Under ice-cooling this was extracted with ethyl acetate the solvent was distilled off
来源 ID: ord-53e03c4968f94623a0aa01cae23e16bf反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of phenylboronic acid (3.4 g, 28.7 mmol), 2,6-dibromoanisole (22.3 g, 83.8 mmol, 3 equiv.) and palladium tetrakistriphenylphosphine (0.6 g) in ethylene glycol dimethyl ether (50 mL) and a solution of potassium carbonate (10.8 g, 0.078 mol) in water (50 mL) were kept at reflux under nitrogen with good stirring overnight. After cooling, the reaction mixture was partitioned between ethyl acetate (800 mL) and water (400 mL). The organic phase was washed with water (2×400 mL), dried over sodium sulfate and filtered. The solvent was removed in vacuo and the residue was chromatographed on silica (360 g) with heptane (5 L) to afford 6.55 g of pure product (87%). at reflux under nitrogen After cooling the reaction mixture was partitioned between ethyl acetate (800 mL) and water (400 mL) The organic phase was washed with water (2×400 mL) dried over sodium sulfate filtered The solvent was removed in vacuo the residue was chromatographed on silica (360 g) with heptane (5 L)
来源 ID: ord-5a56c11120814a7aaa5d0cc913386c4c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 2,6-dibromophenol (25 g, 0.099 mol), powder potassium carbonate (28 g, 0.2 mol, 2 equiv) and dimethyl sulfate (12.6 g, 0.099 mol) in acetonitrile (400 mL) was kept at reflux with good stirring for 4 hr. After cooling, the solids were removed by filtration and the solvent was removed in a rotary evaporator. The residue was taken in 2:1 heptane/ethyl acetate mixture (800 mL) and washed with water (2×400 mL). The organic layer was dried over sodium sulfate, filtered and the solvent was removed in a rotary evaporator, leaving almost pure 1 (15.5 g, 96%). at reflux After cooling the solids were removed by filtration the solvent was removed in a rotary evaporator washed with water (2×400 mL) The organic layer was dried over sodium sulfate filtered the solvent was removed in a rotary evaporator
来源 ID: ord-99facb1a8b3543a985521627d332adbc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 2,6-dibromophenol (25 g, 0.099 mol), powder potassium carbonate (28 g, 0.2 mol, 2 equiv) and dimethyl sulfate (12.6 g, 0.099 mol) in acetonitrile (400 mL) was kept at reflux with good stirring for 4 hr. After cooling, the solids were removed by filtration and the solvent was removed in a rotary evaporator. The residue was taken in 2:1 heptane/ethyl acetate mixture (800 mL) and washed with water (2×400 mL). The organic layer was dried over sodium sulfate, filtered and the solvent was removed in a rotary evaporator, leaving almost pure 1 (15.5 g, 96%). at reflux After cooling the solids were removed by filtration the solvent was removed in a rotary evaporator washed with water (2×400 mL) The organic layer was dried over sodium sulfate filtered the solvent was removed in a rotary evaporator
来源 ID: ord-99facb1a8b3543a985521627d332adbc反应条件: temp:40.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a THF solution of 2,6-dibromoanisole (10 g, 37.6 mmol) was added Mg (0.90 g, 37.6 mmol), and the mixture was heated and stirred at 40° C. Under ice-cooling, n-heptanal (47.2 g, 41.3 mmol) was added dropwise. Aqueous hydrochloric acid solution was added to the reaction mixture, this was extracted with ethyl acetate, and the solvent was distilled off to obtain 8.95 g of a compound (1). the mixture was heated Under ice-cooling this was extracted with ethyl acetate the solvent was distilled off
来源 ID: ord-53e03c4968f94623a0aa01cae23e16bf反应条件: temp:40.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a THF solution of 2,6-dibromoanisole (10 g, 37.6 mmol) was added Mg (0.90 g, 37.6 mmol), and the mixture was heated and stirred at 40° C. Under ice-cooling, n-heptanal (47.2 g, 41.3 mmol) was added dropwise. Aqueous hydrochloric acid solution was added to the reaction mixture, this was extracted with ethyl acetate, and the solvent was distilled off to obtain 8.95 g of a compound (1). the mixture was heated Under ice-cooling this was extracted with ethyl acetate the solvent was distilled off
来源 ID: ord-53e03c4968f94623a0aa01cae23e16bf反应条件: temp:40.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a THF solution of 2,6-dibromoanisole (10 g, 37.6 mmol) was added Mg (0.90 g, 37.6 mmol), and the mixture was heated and stirred at 40° C. Under ice-cooling, n-heptanal (47.2 g, 41.3 mmol) was added dropwise. Aqueous hydrochloric acid solution was added to the reaction mixture, this was extracted with ethyl acetate, and the solvent was distilled off to obtain 8.95 g of a compound (1). the mixture was heated Under ice-cooling this was extracted with ethyl acetate the solvent was distilled off
来源 ID: ord-0586628f68394c568875f29b5148eba6反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1c4d2ee9c9804bc2ae3b03e7907aaeef反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-07fcf513449d4b0eab38bd2631d7c44ePubChem References
以下资料来自该化合物的公开数据库参考记录。
