反应 #3871449
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-1e3b277547764145a871de38ebbf2562暂无可渲染的结构数据
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2-溴苯乙炔(CAS 766-46-1)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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6 条反应 · 6 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1e3b277547764145a871de38ebbf2562反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 1M Lithium hexamethyldisilazide solution (6 mL) was added to 1-bromo-2-ethynylbenzene (1 g) in 20 mL tetrahydrofuran at room temperature, and the reaction was stirred 30 minutes. (CH3)2SO4 (0.58 mL) was added and the reaction was stirred 30 minutes. The reaction was poured into 20 mL water, extracted with 2×50 mL ether, and the combined organic layers were dried over Na2SO4, filtered, and the filtrate was concentrated. the reaction was stirred 30 minutes extracted with 2×50 mL ether the combined organic layers were dried over Na2SO4 filtered the filtrate was concentrated
来源 ID: ord-b4e0c436c99f4c95aad5f5ead95384fe反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 1M Lithium hexamethyldisilazide solution (6 mL) was added to 1-bromo-2-ethynylbenzene (1 g) in 20 mL tetrahydrofuran at room temperature, and the reaction was stirred 30 minutes. (CH3)2SO4 (0.58 mL) was added and the reaction was stirred 30 minutes. The reaction was poured into 20 mL water, extracted with 2×50 mL ether, and the combined organic layers were dried over Na2SO4, filtered, and the filtrate was concentrated. the reaction was stirred 30 minutes extracted with 2×50 mL ether the combined organic layers were dried over Na2SO4 filtered the filtrate was concentrated
来源 ID: ord-b4e0c436c99f4c95aad5f5ead95384fe反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 1M Lithium hexamethyldisilazide solution (6 mL) was added to 1-bromo-2-ethynylbenzene (1 g) in 20 mL tetrahydrofuran at room temperature, and the reaction was stirred 30 minutes. (CH3)2SO4 (0.58 mL) was added and the reaction was stirred 30 minutes. The reaction was poured into 20 mL water, extracted with 2×50 mL ether, and the combined organic layers were dried over Na2SO4, filtered, and the filtrate was concentrated. the reaction was stirred 30 minutes extracted with 2×50 mL ether the combined organic layers were dried over Na2SO4 filtered the filtrate was concentrated
来源 ID: ord-186b10620d4542f3ba0c98b4dd43f4e4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 1M Lithium hexamethyldisilazide solution (6 mL) was added to 1-bromo-2-ethynylbenzene (1 g) in 20 mL tetrahydrofuran at room temperature, and the reaction was stirred 30 minutes. (CH3)2SO4 (0.58 mL) was added and the reaction was stirred 30 minutes. The reaction was poured into 20 mL water, extracted with 2×50 mL ether, and the combined organic layers were dried over Na2SO4, filtered, and the filtrate was concentrated. the reaction was stirred 30 minutes extracted with 2×50 mL ether the combined organic layers were dried over Na2SO4 filtered the filtrate was concentrated
来源 ID: ord-214b989ff8ab47cca24132ac31c32c2c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 1M Lithium hexamethyldisilazide solution (6 mL) was added to 1-bromo-2-ethynylbenzene (1 g) in 20 mL tetrahydrofuran at room temperature, and the reaction was stirred 30 minutes. (CH3)2SO4 (0.58 mL) was added and the reaction was stirred 30 minutes. The reaction was poured into 20 mL water, extracted with 2×50 mL ether, and the combined organic layers were dried over Na2SO4, filtered, and the filtrate was concentrated. the reaction was stirred 30 minutes extracted with 2×50 mL ether the combined organic layers were dried over Na2SO4 filtered the filtrate was concentrated
来源 ID: ord-b4e0c436c99f4c95aad5f5ead95384fePubChem References
以下资料来自该化合物的公开数据库参考记录。
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