反应 #4161942
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-cc8ad679a0a54aa6904fd8975467507b暂无可渲染的结构数据
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替诺福韦艾拉酚胺杂质79(CAS 102-10-3)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-cc8ad679a0a54aa6904fd8975467507b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f70cc3c8bdfe43fa9f0ed50433fc2a2a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-07b7ae7d3ff24f469b1ab6c5eb8dacfa反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7e91ff195938445a8245c8a52f9e73d5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ef4ef76d98de480c8ccba993b260404f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-de80c97527fd4b2db401eb2631bdbd46反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fca9407dee74421db82ec26b9cc0b273反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of diphenylphosphite (2.25 mL) in dichloromethane at 0° C. was added t-butylbromoacetate (1.48 mL) followed by triethylamine (1.95 mL). The mixture was stirred at 0° C. for 15 min and then at rt for 1 h before being quenched with water and extracted into ethyl acetate, dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography eluting with hexane/ethyl acetate to give the title compound. 1H NMR (500 MHz, CDCl3): δ 7.40-7.18 (m, 10H); 3.22 (s, 1H); 3.18 (s, 1H); 1.50 (s, 9H). at rt for 1 h before being quenched with water extracted into ethyl acetate dried over MgSO4 concentrated The residue was purified by silica gel chromatography eluting with hexane/ethyl acetate
来源 ID: ord-65ac710e789949a5880f74f2b654d1e1反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-pyridinecarboxyaldehyde (1.07 g, 10 mmol) and allylamine (0.61 g, 10 mmol) in ether (30 ml) was added anhydrous sodium carbonate (2.76 g). The solution was stirred at r.t. overnight, then sodium carbonate was filtered off. To the reaction mixture, diphenylphosphite (2.34 g, 10 mmol) and triethylamine (1.01 g, 10 mmol) were added with cooling over an ice-water bath. It was stirred at r.t. overnight. After removal of the solvent an oily residue was obtained which was chromatographed (1:1 Petroleum ether/ethyl acetate) to give 2.85 g (65%) as an oil. sodium carbonate was filtered off with cooling over an ice-water bath It was stirred at r.t. overnight After removal of the solvent an oily residue was obtained which was chromatographed (1:1 Petroleum ether/ethyl acetate) to give 2.85 g (65%) as an oil
来源 ID: ord-2813e4c507bd41528b6ee5ed13fdffab反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-cc8ad679a0a54aa6904fd8975467507b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f70cc3c8bdfe43fa9f0ed50433fc2a2a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f70cc3c8bdfe43fa9f0ed50433fc2a2aPubChem 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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