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openreactiondata ↗doi:10.1039/C8SC04228D
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来源 ID: ord-13e4cecb6bd341b8a356e4baec51c648暂无可渲染的结构数据
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3-溴-4-甲氧基苯甲醛(CAS 34841-06-0)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-13e4cecb6bd341b8a356e4baec51c648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-0688361ad893483bb4c607c010fdaf98反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-bb7e44b955084abf8b757247f9ef6cf4反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of sodium ethylate in ethanol (prepared from sodium (1.92 g; 83.70 mmol) and EtOH (40 mL)) was added dropwise to a cold (−10° C.) solution of 3-bromo-p-anisaldehyde (4 g; 18.60 mmol) and ethyl azidoacetate (ABCR, 27.80 ml; 46.50 mmol) in EtOH (60 mL). After the end of the addition, the reaction mixture was warmed up to 0° C. and stirred at RT for 5 hours. The heterogenous mixture was poured onto ice and stirred for 30 minutes. The solid was collected by filtration and dried under high vacuum. The solid was taken up in xylenes (60 mL) and heated to reflux for 3 hours. The solvent was evaporated and the residue was purified by silica column chromatography (c-Hexane/ethyl acetate, 80/20) to give the title compound as a pale yellow solid. 1H NMR (DMSO-d6) δ 11.87 (s, 1H), 7.89 (s, 1H), 7.05 (s, 1H), 6.98 (s, 1H), 4.31 (q, J=7 Hz, 2H), 3.85 (s, 3H), 1.32 (t, J=7 Hz, 3H). HPLC (Method A), Rt 4.28 min (Purity: 98.1%). LC/MS (Method B): 297.2 (M+H)+. After the end of the addition The heterogenous mixture was poured onto ice stirred for 30 minutes The solid was collected by filtration dried under high vacuum heated to reflux for 3 hours The solvent was evaporated the residue was purified by silica column chromatography (c-Hexane/ethyl acetate, 80/20)
来源 ID: ord-31cfe72e145c442c9af98cb8cdb4e709反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Addition of 3-bromo-4-methoxybenzaldehyde to acetonitrile gave 3-(3-bromo-4-methoxyphenyl)-3-hydroxypropanenitrile as a pale orange oil. Yield (10.32 g, 96%): 1H NMR (400 MHz, DMSO-d6) δ 7.58 (d, J=2.0 Hz, 1H), 7.35 (dd, J=8.8, 2.0 Hz, 1H), 7.07 (d, J=8.8 Hz, 1H), 5.93 (d, J=4.4 Hz, 1H), 4.85-4.81 (m, 1H). 3.81 (s, 3H), 2.86 (ABd, J=16.4, 4.8 Hz, 1H), 2.79 (ABd, J=16.8, 6.8 Hz, 1H).
来源 ID: ord-7fac66f00e2340bfb00ffcedc597dcc8反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-13e4cecb6bd341b8a356e4baec51c648PubChem References
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