反应 #4023393
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-f1f431a7cf98457eb93da3a0d7daa89d暂无可渲染的结构数据
C1CCOC(C1)OCCN=[N+]=[N-]产品信息
2-(2-叠氮乙氧基)氧烷(CAS 835625-50-8)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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7 条反应 · 7 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f1f431a7cf98457eb93da3a0d7daa89d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f1f431a7cf98457eb93da3a0d7daa89d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The reaction was carried out similarly as described in the preparation of compound 101, using compound 432 (2.06 mmol) and compound 408 (2.06 mmol). The crude product was purified by continuous gradient flash chromatography using EtOAc/petroleum ether (40-60) 50:50 to 50:50 as the eluent to afford the title compound. The crude product was purified by continuous gradient flash chromatography
来源 ID: ord-b5925b0ecdc84490b065c6674422a3a9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The reaction was carried out similarly as described in the preparation of compound 101, using compound 427 (0.42 mmol) and compound 408 (0.42 mmol). The crude product was purified by continuous gradient flash chromatography using EtOAc/petroleum ether (40-60) 20:80 to 60:40 as the eluent to afford the title compound as light orange foam. The crude product was purified by continuous gradient flash chromatography
来源 ID: ord-9bea2da4d0cc488b9b3115b887389233反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The reaction was carried out similarly as described in the preparation of compound 408, using toluene-4-sulfonic acid 2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester (37.8 mmol). The crude product was purified by continuous gradient flash chromatography using EtOAc/petroleum ether (40-60) 0:100 to 20:80 as the eluent to afford the title compound as colourless foam. The crude product was purified by continuous gradient flash chromatography
来源 ID: ord-abffc33633e94169875634d46af8b233反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 2-(2-bromo-ethoxy)-tetrahydro-pyran (1.00 mL, 6.62 mmol), NaN3 (4.34 g, 66 mmol) and tetrabutylammonium iodide (245 mg, 0.66 mmol) in DMF (7.0 mL) was stirred at RT for 18 h. The reaction mixture was poured into a mixture of EtOAc/water. The organic phase was washed with water, brine and then dried (MgSO4), filtered and concentrated in vacuo to give the crude product. The crude product was purified by continuous gradient flash chromatography using EtOAc/petroleum ether (40-60) 0:100 to 20:80 as the eluent to afford the title compound as colourless oil. The organic phase was washed with water, brine dried (MgSO4) filtered concentrated in vacuo to give the crude product The crude product was purified by continuous gradient flash chromatography
来源 ID: ord-ee53d6f9a5bf41f3b026d03b2a71bebc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f1f431a7cf98457eb93da3a0d7daa89dPubChem 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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