反应 #4142787
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openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-24629dc7034c4e219335d9806a929164暂无可渲染的结构数据
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叠氮乙酸甲酯(CAS 1816-92-8)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-24629dc7034c4e219335d9806a929164反应条件: temp:0.00; pressure:0.00; stir:
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来源 ID: ord-8479535501404375b6306d98c3810ced反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4446efa03c42499992a5e1926a0de115反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7a224499913044319e2c942c092d104d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-Benzyloxybenzaldehyde (10.0 g) and methyl azidoacetate (21.7 g) are dissolved in 157 ml of methanol and cooled to -10° (ice-acetone bath). Then sodium methoxide (43.1 ml, 25% in methanol) is added dropwise such that the reaction temperature does not rise above -5°. After 2 hr, the cooling bath is removed and the reaction is warmed to 20°-25°. When no starting material remains by TLC, the reaction is diluted with ether and washed with saturated aqueous ammonium chloride. The organic layer is washed with water, saline, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Purification by flash column chromatography (hexane to 5% ethyl acetate/hexane) gives the title compound. does not rise above -5° the cooling bath is removed the reaction is warmed to 20°-25° the reaction is diluted with ether washed with saturated aqueous ammonium chloride The organic layer is washed with water, saline dried over anhydrous sodium sulfate concentrated under reduced pressure Purification by flash column chromatography (hexane to 5% ethyl acetate/hexane)
来源 ID: ord-b2d35750dac440d2a14eb940a8644fcd反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: While 23 ml of sodium methoxide (28% solution in methanol) in 40 ml of anhydrous methanol was stirred vigorously, 40 ml of a mixed methanol solution containing 4.0 g (21.1 mmol) of 2,5-dimethoxybenzaldehyde and 9.7 g (84.2 mmol) of methyl azidoacetate was added dropwise at -15° C. After completion of the addition, the reaction mixture was stirred for 2 hours. Then the reaction mixture was poured into a saturated ammonium chloride solution and extracted with ethyl acetate. The extract was washed with water and dried over magnesium sulfate. After distilling off the solvent, the residue was purified by silica gel chromatography (hexane:ethyl acetate=10:1) to provide 3.1 g of methyl 2,5-dimethoxyphenyl-α-azidocinnamate. was added dropwise at -15° C After completion of the addition extracted with ethyl acetate The extract was washed with water dried over magnesium sulfate After distilling off the solvent the residue was purified by silica gel chromatography (hexane:ethyl acetate=10:1)
来源 ID: ord-d3b18866e13a4ceba6cb6fa906dbdb8c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-24629dc7034c4e219335d9806a929164反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-24629dc7034c4e219335d9806a929164PubChem References
以下资料来自该化合物的公开数据库参考记录。
