反应 #4133829
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openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e8ea2283e47e4e328bf6a880a9bac9e1暂无可渲染的结构数据
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1-碘-2-甲氧基苯(CAS 529-28-2)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。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e8ea2283e47e4e328bf6a880a9bac9e1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-27cf2b481e8f4ea0b21c07132f95f6be反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9e7fdca9a73847468404bde8f0d637f4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a4abef4432994ad7a796e6dca6817b59反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7c0c641ed4a6477ebfd4fd4fae808f46反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b17eb868bf7c4a69bba998727b3f9033反应条件: temp:200.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Iodoanisole (1.30 mL, 0.01 mol), 2-hydroxypyridine (0.95 g, 0.01 mol), anhydrous K2CO3 (2.76 g, 0.02 mol) and copper powder (0.0636 g, 0.001 mol) were combined and heated at 200° C. for 2 hr. The reaction mixture was cooled, EtOAc added, and filtered. The filtrate was washed with H2O, aqueous saturated NaHCO3 solution, brine, and dried (Na2SO4). Filtration and concentration gave the title compound after chromatography (silica gel, 2% CH3OH, CH2Cl2). The reaction mixture was cooled filtered The filtrate was washed with H2O, aqueous saturated NaHCO3 solution, brine dried (Na2SO4) Filtration and concentration
来源 ID: ord-4c3a55ba796041aab00b78a70ae21ba3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e8ea2283e47e4e328bf6a880a9bac9e1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e8ea2283e47e4e328bf6a880a9bac9e1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-27cf2b481e8f4ea0b21c07132f95f6be反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-27cf2b481e8f4ea0b21c07132f95f6be反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirred, cold (-78° C.) solution of 2-iodoanisole (2.85 ml, 5.6 g) in 50 ml of tetrahydrofuran under nitrogen was added 10.0 ml of 2.5M n-butyl lithium in hexane. After 15 min. triisopropyl borate (3.38 ml, 4.7 g) was added and the reaction was allowed to come to and remain at room temperature for 1.5 hr. The mixture was poured into an excess of 2N hydrochloric acid and diethyl ether was added. The resulting mixture was stirred vigorously for 30 min. and the phases were separated. The ether layer was washed with aqueous sodium bisulfite until colorless and then with saturated sodium chloride solution and then dried over magnesium sulfate. Concentration of the ether layer gave the crude boronic acid which crystallized from ether to give the title product. was added the phases were separated The ether layer was washed with aqueous sodium bisulfite until colorless and then with saturated sodium chloride solution dried over magnesium sulfate Concentration of the ether layer gave the crude boronic acid which crystallized from ether
来源 ID: ord-9648bcaa93904f84bff8f019a351e1c5PubChem References
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